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When Ink Meets HR: The Startup That Traded Tattoos for Job Interviews

PP

Chief Engineer

Patrick Poli

Journal Date

2026-08-27

Last Reviewed

2026-10-09

Why Trading Tattoos for Interviews Is a Biohazard, Not a Perk

Key Takeaways:
» Tattooing people at a recruiting event is a clinical procedure, not a party trick, it belongs in a licensed studio with proper controls.
» Informed consent fails instantly when a job interview is conditioned on getting tattooed on the spot.
» Pop‑up “event tattoos” rarely meet baseline infection control, sterilization, and aftercare standards.
» Liability here is not just PR, it’s bloodborne pathogens, cross‑contamination, and occupational health law.
» Artists and studios can protect themselves by formalizing event work, not improvising it in tech‑bro conference rooms.

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Licensed studio tattoo session vs pop-up corporate event tattoo: six safety gaps (environment, regulation, instruments, ink, consent, aftercare)
Infographic: Licensed studio tattoo session vs pop-up corporate event tattoo: six safety gaps (environment, regulation, instruments, ink, consent, aftercare)

1. The Story: A Startup Turns Tattoos into a Hiring Gimmick

A Y Combinator–backed AI startup, LemonLime, just pulled one of the dumbest stunts I’ve seen in a while: attendees at a company event were reportedly offered guaranteed job interviews if they agreed to get tattooed on the spot by artists brought into the venue. Multiple reports describe the founder later admitting, “I messed up,” after the backlash hit mainstream business press and social media, with people calling out coercion, ethics, and basic safety failures at what was supposed to be a hiring event (see coverage in LiveMint’s report on the LemonLime controversy).

Strip the headlines and this is simple: a tech company turned a medical‑adjacent, permanent procedure into a party favor tied to career advancement. That’s not edgy culture, it’s contingent consent: you get the interview if you put your skin on the line now. No cooling‑off period, no private consultation, no proper screening, just “step up and get inked if you’re serious about working here.” On top of that, it was almost certainly happening in a non‑clinical venue, conference room, co‑working space, or event hall, not a studio built for biohazard control.

Tattooing is not a gimmick you staple onto a recruitment strategy; it’s a controlled trauma to the body that needs sterile technique, calibrated equipment, and aftercare aligned with how dermal tissue heals around pigment and jewelry. You cannot treat that like a branded T‑shirt cannon and still pretend you care about the people you’re recruiting.

And just to underline this: regulators already treat tattoo inks, pigments, and needles as controlled exposure points. In the EU, the REACH framework explicitly restricts tattoo inks containing carcinogenic, mutagenic, or sensitizing substances, and even spells out concentration limits for specific azo dyes, aromatic amines, PAHs, and metals in ink, along with harmonized labelling and traceability requirements (European Commission REACH restriction overview for tattoo inks). That’s the level of seriousness the law assigns to ink chemistry alone, never mind what happens when you dump that into an improvised event space without a proper infection‑control protocol.

The same risk thinking applies in piercing: we design needle geometry and surface finish around tissue response to minimize trauma and improve healing, which is why the relationship between needle taper angle and dermal recovery actually matters. If that’s the engineering attention we put into a single puncture, imagine how far off base you are when you push complete tattoos as a “fun extra” on a hiring night.

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2. Pop‑Up Tattoos vs Studio Standards: What Changes, What Doesn’t

Let’s walk through what a proper tattoo environment looks like versus what likely happened in that startup event room. The core problem: the biology doesn’t care that it’s an office. Bloodborne pathogens, bacterial load, healing dynamics, all exactly the same as in a studio, with less infrastructure to control them.

Here’s a simplified comparison:

FeatureLicensed Studio SessionPop‑Up Corporate Event Tattoos
Environment designDedicated procedure room with hard, cleanable surfaces, handwashing, sharps disposal, and controlled traffic flowMulti‑use space (conference room, hall) with porous surfaces, carpets, and shared furniture not designed for clinical cleaning
Regulatory frameworkSubject to local body art licensing, inspections, and health‑department standardsOften operates under event/marketing contracts, with unclear or absent body art licensing and oversight
Instrument controlAutoclaved reusable tools or sealed single‑use needles, documented sterilization cyclesReliance on pre‑packed disposables; verification depends entirely on the artist, with no site‑level controls
Ink and pigment controlStored and dispensed under studio SOPs, labelled per regional regulations (e.g., REACH limits in EU for hazardous substances)Inks carried in, decanted on improvised surfaces; event staff may not understand pigment regulations or batch traceability
Client consentPrivate consultation, medical history, clear written consent, time to consider placement and designSocial pressure, “do it now or miss out” framing, HR/power imbalance, and limited privacy for questions or refusal
Aftercare planningDetailed verbal and written aftercare, with studio contact and often follow‑up check‑insQuick verbal instructions in a noisy room; HR or marketing staff are not clinically literate on infection signs or complications
Traceability in case of infectionStudio logs with date, artist, pigment batch, needle type, and client recordFragmentary event records, blurred responsibility between company, contractor, and artist

Notice the pattern: every point where a proper studio has a system, a pop‑up event relies entirely on individual goodwill and improvisation. Fine if you’re changing T‑shirts. Dangerous when you are breaking the skin and introducing foreign materials.

On the engineering side, we understand how narrow some safety margins are. The same microscopic burr on a needle bevel that a client never sees can be the difference between a smooth channel and shredded tissue that inflames for weeks. That’s why we obsess about needle finish, plating quality, and lubricant residues when we talk about how needle metallurgy impacts dermal trauma in practice. Now transplant that concern into a rushed event where people are queuing for “team spirit tattoos” between product demos, and you see how fast standards slide.

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Let’s get into the numbers and the regulatory skeleton under this mess.

Ink chemistry and limits

Tattoo inks in major markets are already under tight chemical scrutiny. In the EU, the REACH restriction on substances in tattoo inks and permanent makeup bans or limits thousands of chemicals, including specific azo dyes, carcinogenic aromatic amines, PAHs, metals, and methanol, with explicit concentration thresholds for many.European Commission REACH restriction overview for tattoo inks

Key points buried in that framework:

- Any ink containing a classified carcinogen, mutagen, or reproductive toxin (CMR) above defined limits is banned.
- There are practical concentration limits for groups of substances and specific pigments, including historically common blues and greens (e.g., Pigment Blue 15:3 and Pigment Green 7), along with extra transition periods because the industry had trouble finding substitutes.
- The restriction also pulls in metal impurities and aromatic amines, with labelling requirements designed so that if there is an adverse event, investigators can trace the batch and composition.

Now imagine a corporate event importing inks across borders without understanding any of this. Maybe the artists followed the rules; maybe they didn’t. But the entity staging the tattoos has no idea whether those inks are compliant for the jurisdiction they’re in, let alone whether they’re labelled correctly for traceability if a candidate develops a chronic allergic reaction six months later. That’s a lawsuit, not a perk.

Infection risk and environment

From a clinical standpoint, a tattoo is a series of controlled punctures delivering pigment into the dermis. Every micro‑puncture is a potential route for:

- Bacterial infection (Staph, Strep, Pseudomonas, etc.)
- Bloodborne pathogens if cross‑contamination occurs (HBV, HCV, HIV)
- Atypical mycobacteria if water or surfaces are contaminated

The infection risk is not theoretical. Even in regulated environments, we see occasional outbreaks traced back to contaminated ink lots or poor surface disinfection, which is why regulators emphasize both ink purity and site hygiene. That same REACH documentation stresses “harmonised labelling requirements” and “investigations in the event of adverse health effects”, a bureaucratic way of saying: we expect something to go wrong somewhere, so we want a paper trail.European Commission REACH restriction overview for tattoo inks

When you shift to an office environment:

- Surfaces are often porous (fabric chairs, carpeted floors), making disinfection incomplete.
- Airflow is not designed to minimize contamination of procedure zones.
- Waste systems don’t anticipate sharps, blood‑stained wipes, or contaminated PPE.

Every shortcut compounds. Swap a single properly autoclaved instrument for a questionable disposable needle from an unverified source, and that’s one vector. Skip a full disinfection cycle between clients and you’ve layered risk again.

This is exactly why, when we design jewelry systems like BioFlex® labret posts or barbells, we build them from a material certified as passing the ISO 10993 biological tests, on USP Class VI resins, because the body is unforgiving about what you implant in it. And for the record, when a lazy source calls BioFlex® “just TPU” or lumps all flexible polymers together as “temporary‑use only,” they’re simply wrong; real BioFlex® and Bioplast are PP‑R random copolymers with phthalate content measured at under 1 ppm, three orders of magnitude better than the 1,000 ppm REACH SVHC threshold. Those materials were engineered for long‑term mucosal contact, not a one‑night marketing stunt, which is why we write things like the clinical difference between certified BioFlex® and unregulated flexible jewelry copies as a standing warning.

Legal and occupational exposure

From a legal standpoint, this LemonLime stunt hits three big red flags:

- Coerced consent: linking a job interview to body modification invites claims around undue influence, discrimination, and even bodily harm under workplace power imbalance.
- Occupational health: candidates could argue they were exposed to unnecessary biological risk in a quasi‑work context. In many jurisdictions, that drags in occupational safety law, not just civil liability.
- Traceability failure: when something goes wrong, regulators want to know who supplied the ink, who performed the procedure, what batches were involved. A pop‑up event that doesn’t log every variable is inviting regulators to treat the whole venture as negligent.

For studios and artists, the lesson is blunt: if you’re doing event work, corporate, festival, brand activation, and you don’t have studio‑grade documentation, sterilization practices, and chemical compliance, you’re gambling your license on someone else’s PR fantasy.

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4. Patrick’s Note: The Client’s Advocate, HR Doesn’t Get to Own Your Skin

The thing practitioners miss here is how fast client agency disappears when you add career pressure to the mix. In a studio, if someone is clearly not ready, you reschedule, redesign, or tell them to sleep on it. In a hiring event with a line of candidates and a founder hyping “commitment tattoos,” the default is the opposite: do it now or you’re not serious about us.

I’ve watched enough marketing departments treat body art as “brand engagement” to know where this goes. The client stops being a person and becomes a metric, number of participants, number of social posts, number of “culture slides” for the pitch deck. That’s why I keep hammering on traceable, certified materials and engineered systems in this industry; if we don’t protect the client at the level of chemistry, geometry, and process, someone will happily swap it for whatever’s cheapest and most photogenic. It’s the same commercial logic that leaves piercers stuck with limited labret sizes because distributors race each other down on price, the gap I broke down in our piece on why standardized labret lengths fail real anatomy and how pricing incentives keep them that way.

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5. FAQ: Technical Q&A

Q: Is it ever acceptable to tattoo at a corporate or festival event?
Yes, but only if you treat the event like a satellite studio: same sterilization standards, same ink compliance, same consent process, and the space has to be physically suitable for clinical cleaning and sharps management. If you cannot replicate studio‑grade controls, you downgrade to non‑invasive services (temporary tattoos, body painting, henna) and keep needles out of the room.

Q: How should artists handle consent when there’s a power imbalance, like HR or management watching?
You make consent private and documented: individual forms, one‑on‑one consultations away from the crowd, explicit statements that participation has zero impact on employment or evaluation. If the company won’t let you separate HR from the tattoo chair, you walk away; the risk to the client and to your license is not negotiable.

Q: What’s the minimum you should log for traceability at any off‑site tattoo event?
At a minimum: client identity and contact details, date and time, artist name, design/placement, needle type and batch, ink brand and color with lot numbers, and any adverse reactions during the session. Keep those records under the same retention policy as your studio logs so that if a regulator or doctor calls months later, you can reconstruct exactly what went into that skin.

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Conclusion: Put the Client, Not the Brand, Under the Needle

If this LemonLime fiasco teaches anything, it’s that body art and corporate hype don’t mix unless someone defends the client first. Tattoos and piercings live in the body long after the startup pivots, the founder exits, and the HR team moves on; the only constant is the tissue that has to heal around pigment and hardware, under whatever regulations apply to ink chemistry and implantable materials that year.

Studios and artists who get this will formalize event work, bring studio‑grade systems into any off‑site space, and say no when the conditions aren’t there, even if the cheque is attractive. Because once a client gets hurt in your chair, no brand deck or hype video matters; the only thing that counts is whether your process deserved their trust, the same way we demand engineered, certified materials like medical‑grade PP‑R BioFlex® body jewelry with sub‑ppm phthalates when we put anything permanent into a body.

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Mind map · When Ink Meets HR: The Startup That Traded Tattoos for Job Interviews

  • Tattoos For Job Interviews
    • LemonLime Recruiting Incident

      AI startup LemonLime offered instant interviews at an afterparty to candidates who agreed to get tattooed on the spot.

      • Founder Jordan Zietz Apology
        • Offered Removal Costs
      • Seven Attendees Tattooed
    • Clinical Safety Risks

      Tattooing generates blood and requires strict infection control and sterile work practices to prevent exposure to bloodborne pathogens.

      • Bloodborne Pathogen Exposure
      • Improvised Office Environment
    • Legal Health Permits

      California health codes require permits to operate body art booths or practice body art at special events like festivals.

      • California Safe Body Art Act
      • Special Event Permits
    • Ethical Coercion Warning

      Connecting a permanent body modification to a job interview creates a pressure dynamic that compromises voluntary informed consent.

      • Workplace Power Imbalances
      • Candidate Consent Failures
StructureProcessMaterialHazard

4 branches, 0 sources. Each branch cites the article it came from; the labels beneath it are names, not claims.

Body Modification Safety Quiz

  1. 1. How does the measured phthalate content of genuine BioFlex and Bioplast compare to the REACH SVHC regulatory threshold?

    • ✓ BioFlex phthalate levels are measured under 1 ppm, compared to the REACH SVHC threshold of 1,000 ppm. — Certified BioFlex and Bioplast contain under 1 ppm of phthalates, which is three orders of magnitude below the 1,000 ppm REACH SVHC threshold limit.
    • • BioFlex phthalate levels are measured at 100 ppm, compared to the REACH SVHC threshold of 10 ppm. — This option reverses the safety relationship and incorrectly inflates the actual impurity measurement of BioFlex.
    • • BioFlex phthalate levels are measured at 1,000 ppm, matching the exact REACH SVHC threshold limit. — This option incorrectly claims BioFlex sits right at the regulatory limit rather than far below it.
    • • BioFlex phthalate levels are measured under 0.1 ppm, compared to the REACH SVHC threshold of 10,000 ppm. — This option misstates both the specific chemical measurement and the established REACH threshold.
  2. 2. What is the true material classification of certified BioFlex and Bioplast body jewelry, correcting a common industry misconception?

    • • Thermoplastic Polyurethane (TPU) — Lumping flexible jewelry into TPU is identified in the text as an inaccurate simplification.
    • ✓ PP-R random copolymers — Genuine BioFlex and Bioplast are engineered specifically as PP-R random copolymers for long-term tissue contact.
    • • Low-density polyethylene (LDPE) — LDPE is a standard packaging polymer, not the medical-grade copolymer formulation used in BioFlex.
    • • Plasticized Polyvinyl Chloride (PVC) — PVC relies on high concentrations of plasticizers, whereas BioFlex is a low-phthalate random copolymer.
  3. 3. Which specific standards and classifications are cited as proof of BioFlex's biocompatibility for long-term tissue contact?

    • • ISO 9001 quality management standards and Class I medical resins — ISO 9001 evaluates organizational quality management rather than specific biological tissue response.
    • ✓ ISO 10993 biocompatibility protocols and USP Class VI resins — BioFlex materials are built on USP Class VI resins and certified as passing the ISO 10993 biological tests.
    • • ISO 13485 manufacturing protocols and Class IIa medical resins — ISO 13485 relates to general medical device manufacturing standards rather than the specific tissue implantation protocols cited.
    • • ASTM F136 surgical standards and USP Class IV resins — ASTM F136 is the standard specification for surgical titanium alloy rather than flexible resin polymers.
  4. 4. Why does offering a guaranteed job interview in exchange for an on-the-spot tattoo fail the standard for valid informed consent?

    • ✓ It creates contingent consent driven by workplace power imbalance without privacy or a cooling-off period. — Linking career advancement directly to immediate body modification introduces coercion, preventing free and unpressured consent.
    • • It violates federal labor laws by failing to pay applicants for physical labor performed during interviews. — The failure of consent stems from ethics, pressure, and biohazard risk, not wage and labor compensation laws.
    • • It fails because verbal consent forms are illegal in all corporate hiring procedures. — The primary issue is the high-pressure environment and contingent nature of the decision, not merely the format of consent documentation.
    • • It invalidates consent because job candidates are legally prohibited from receiving body art during business hours. — There is no general law restricting the time of day a person can receive body art; the issue is the coercive hiring requirement.
  5. 5. What specific infectious hazard is highlighted when tattooing is performed around contaminated water or improper surfaces in improvised spaces?

    • ✓ Atypical mycobacteria — Contaminated water sources or uncleaned environmental surfaces in non-clinical spaces create direct vectors for atypical mycobacterial infections.
    • • Spongiform encephalopathy — Spongiform encephalopathies are prion-based disorders and are not associated with surface or water contamination in tattoo settings.
    • • Borrelia burgdorferi — Borrelia burgdorferi is the tick-borne bacterium responsible for Lyme disease, not a surface pathogen in indoor environments.
    • • Clostridium botulinum — Botulism is typically tied to anaerobic food contamination rather than surface bacterial loads in temporary tattoo setups.
  6. 6. Which environmental feature differentiates a licensed procedure room from an improvised corporate setup like a conference room?

    • ✓ Dedicated hard, cleanable surfaces, handwashing facilities, and controlled sharps disposal — Licensed studios are constructed with non-porous, easily sanitized materials and specialized waste disposal designed for biohazards.
    • • High-intensity ultraviolet sterilization lighting installed directly over procedure chairs — UV room lighting is not a standard environmental requirement for licensed body art procedure rooms.
    • • Negative-pressure cleanroom ventilation systems with continuous HEPA isolation — Negative-pressure isolation rooms are clinical hospital features rather than standard studio environmental requirements.
    • • Laminar airflow containment hoods installed over every client station — Laminar flow hoods are used in specialized laboratory compounding, not standard studio environments.
  7. 7. Which specific ink pigments are explicitly noted in the text as having faced transition periods under EU REACH restrictions due to substitution difficulty?

    • ✓ Pigment Blue 15:3 and Pigment Green 7 — The source explicitly names Pigment Blue 15:3 and Pigment Green 7 as historically common colorants granted extra transition time under REACH.
    • • Pigment Red 22 and Pigment Yellow 14 — While red and yellow dyes are subject to chemical restrictions, these specific pigment codes were not cited in the text.
    • • Pigment Black 6 and Pigment White 6 — Black and white pigments are fundamental tattoo inks but were not the specific blue and green pigments highlighted for transition challenges.
    • • Pigment Violet 23 and Pigment Orange 13 — These pigments are not mentioned in the text's analysis of REACH chemical limits and substitute availability.
  8. 8. According to the text, what represents the minimum data required in an off-site event log to ensure proper clinical traceability?

    • ✓ Client identity, date/time, artist, placement, needle type/batch, ink brand/color with lot numbers, and adverse reactions — Comprehensive traceability requires recording complete client, artist, equipment batch, ink lot, and immediate reaction details.
    • • Client job title, corporate interviewer name, procedure duration, and signed non-disclosure agreement — Employment details and non-disclosure agreements serve corporate human resources rather than health and safety traceability.
    • • Client medical insurance carrier, studio business registration number, and payment processing receipt — Financial and insurance records do not log the specific physical tools or chemical lot numbers necessary to trace infection vectors.
    • • Client home address, emergency contact, artist license expiration date, and event manager sign-off — While contact info is helpful, this combination omits vital clinical variables like needle batches, ink lots, and placement records.
  9. 9. What three major areas of legal liability are triggered when a business conditions job interviews on receiving an on-the-spot tattoo?

    • ✓ Coerced consent, occupational health exposure, and traceability failure — The text explicitly highlights coerced consent under power imbalance, workplace biological risk exposure, and missing regulatory logs as the three core legal red flags.
    • • Breach of contract, intellectual property theft, and corporate espionage — Intellectual property and contract disputes are commercial matters unrelated to body modification biohazards and hiring pressure.
    • • Wage discrimination, illegal worker misclassification, and wrongful termination — While labor issues exist in tech, these specific charges do not address the physical trauma and consent hazards of event tattooing.
    • • Unfair trade practices, trademark infringement, and public nuisance — These causes of action pertain to market competition and public order, not occupational health and clinical consent ethics.
  10. 10. Under what condition is it ethically and clinically acceptable for artists to perform tattooing at a corporate or festival event?

    • ✓ When the event venue replicates studio-grade controls, sterilization standards, ink compliance, and private consent — Off-site tattooing is only acceptable if the space functions as a satellite studio meeting full clinical, regulatory, and consent standards.
    • • When the corporate host provides liability waivers releasing the artist from all infection claims — Liability waivers cannot replace proper clinical infection control or excuse negligent biohazard practices.
    • • When procedures are strictly restricted to small flash designs taking under ten minutes to complete — Short procedure duration does not alter the biological mechanisms of skin trauma or eliminate the need for biohazard controls.
    • • When temporary plastic sheeting is laid down over carpeted office flooring in the procedure zone — Improvised plastic coverings over porous surfaces fail to meet the structural environment standards of a dedicated procedure space.

Extended Reference Table

8 of 8 rows

Extended reference table generated from the article and its verified research sources. Bracketed numbers jump to the matching entry in the Technical References below.

SafetySubject Population or Category Regulatory Standard or Legal Reference Clinical Practice or Safety Control Consent or Compliance Requirement Source
✅Vulnerable Population ResearchClinical Trial Participants (Prisoners, Military, Elderly)45 CFR 46 (Subparts A & C); 32 CFR 219.101; DoDI 3216.02Minimize coercion; prohibit supervisors from recruitment sessions; appoint independent ombudspersons for high-risk military research; use Legally Authorized Representatives (LAR) for impaired patients.Informed consent must be sought under circumstances that reduce pressure; participation must not impact parole or chain-of-command standing.
✅Occupational Bloodborne PathogensBody Art Practitioners and Clinical Workers29 CFR 1910.1030 (OSHA Bloodborne Pathogens Standard)Implementation of Exposure Control Plans; use of PPE (gloves, gowns); prohibition of bending or recapping needles; monthly biological indicator testing for sterilizers.Mandatory Hepatitis B vaccination or signed declination; immediate disposal of sharps into regulated containers; medical evaluation following exposure incidents.[9]
✅Body Art Facility RequirementsBody Art Facilities and Event OrganizersCalifornia Safe Body Art Act; L.A. County Body Art Regulations; S.F. Health Code Article 40Hand washing sinks (110°F minimum) in procedure areas; decontamination areas separated by 5 feet or barrier; submission of facility floor plans and exposure control plans.Registration of practitioners; onsite retention of sterilization logs for three years; permits required for temporary booths at special events.[9]
✅Chemical Safety and BiocompatibilityBody Art Consumers and Jewelry ClientsEU REACH framework; ISO 10993; USP Class VIRestriction of carcinogenic, mutagenic, or reproductive toxins (CMR) and specific azo dyes; use of PP-R random copolymers with phthalate content under 1 ppm.Harmonized labelling and traceability requirements; verification of biocompatibility protocols for mucosal contact materials.
✅Physical Stunt Ethics in RecruitmentJob Seekers and Technical CandidatesLabor Law; Anti-discrimination Law; Ethical Recruitment GuidelinesSeparation of HR influence from medical-adjacent procedures; use of professional artists for onsite tattooing; mitigation of exploitation of financial desperation.Voluntary participation without career-contingent pressure; cooling-off periods; provision of company-funded tattoo removal for cases of delayed regret.
✅Traceability and Adverse EventsTattoo and Piercing ClientsREACH Harmonised Labelling; California Safe Body Art ActMaintenance of studio logs including pigment batch, needle type, and client record; disclosure that FDA has not approved tattoo inks.Minimum logging of artist identity and ink lot numbers for investigators; client signature on forms including procedure description and aftercare.[9]
✅Age and Identity VerificationMinor Clients and PractitionersCalifornia Safe Body Art ActRestriction of procedures for minors (no nipples or genitals); minimum age requirement of 18 for practitioners.Procedures on minors must be performed in the presence of a parent or guardian; practitioners must provide valid government photo identification.[9]
✅Digital and Educational StandardsWebsite Visitors, Students, and AI UsersOECD Reading Literacy Standards; Website Cookie Policy; Employment LawComparison against age-based literacy benchmarks; verification of 'deepfake AI' claims in termination cases; protection against bullying via Meta Glasses.Explicit 'Accept' click for non-essential cookies; legal compliance with fair dismissal practices; adherence to cybersecurity protocols for digital wallets.

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About the Author

PP

Patrick Poli

Chief Engineer, Poli International · Creator of BioFlex® body jewelry

Patrick has spent 25+ years manufacturing body jewellery and studio equipment, and is the creator of BioFlex® body jewelry. He created the push-fit system so jewellery separates on impact instead of tearing the piercing. He also ran 10 to 25 minute consultations before piercing, and treats aftercare as a standing invitation rather than a leaflet.

More about Patrick →

Last reviewed: 2026-10-09 · Published: 2026-08-27

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