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FDA 510(k)

Collagen P.I.N. (Percutaneous Induction Needling)

K-Number: K222199 · 2022-10-21

ApplicantInduction Therapies, LLC
Decision Date2022-10-21
Product CodeQAI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Collagen P.I.N. (Percutaneous Induction Needling) is the device name listed in this FDA 510(k) record. The listed applicant is Induction Therapies, LLC. It received FDA 510(k) clearance on 2022-10-21 under 510(k) number K222199. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Collagen P.I.N. (Percutaneous Induction Needling)?

Collagen P.I.N. (Percutaneous Induction Needling) is a medical device that received FDA 510(k) clearance on 2022-10-21. The listed applicant is Induction Therapies, LLC. The 510(k) number is K222199.

When did Collagen P.I.N. (Percutaneous Induction Needling) receive FDA 510(k) clearance?

Collagen P.I.N. (Percutaneous Induction Needling) received FDA 510(k) clearance on 2022-10-21, under 510(k) number K222199.

Who is the listed applicant for Collagen P.I.N. (Percutaneous Induction Needling)?

The FDA 510(k) record lists Induction Therapies, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Collagen P.I.N. (Percutaneous Induction Needling)?

The FDA product code for Collagen P.I.N. (Percutaneous Induction Needling) is QAI.

Related Devices (Code: QAI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K252591Automatic Micro Needle System (CODE-X)Woorhi Mechatronics Co., Ltd.K253002SkinStylus SteriLock MicroSystem (MP1209SL)Esthetic Medical, Inc.K252752ellacor System with Micro-Coring TechnologyCytrellis Biosystems, Inc.K253153SER Pen Carain MicroSystem (MP1209SP)Su-Ko Technologies, LLCK243800PRO Pen Microneedling System (6883)Dermalogica, LLCK243143E-PEN (E-PEN)Bomtech Electronics Co., Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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