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Collagen P.I.N.

FDA UDI

Class II (US FDA UDI)

by Induction Therapies, Llc

Identity

Trade Name
Collagen P.I.N. FDA UDI
Generic Name
Cosmetic micro-needling electronic handpiece cartridge, professional FDA UDI
Device Name
24 Pack - 36 Pin Microneedling Cartridge FDA UDI
Model / Reference
1 FDA UDI
Description
24 Pack - 36 Pin Microneedling Cartridge FDA UDI

Identifiers

Primary DI / UDI-DI
00850021673031 FDA UDI
510(k) Number
K222199 FDA UDI
FDA Product Code
QAI FDA UDI
GMDN Term
Cosmetic micro-needling electronic handpiece cartridge, professional FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4430 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Cosmetic micro-needling electronic handpiece cartridge, professional

Collagen P.I.N. by Induction Therapies, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic micro-needling electronic handpiece cartridge, professional.

Cleared under the same submission

K222199 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Induction Therapies, Llc

Sources (1)

  • FDA UDI 5da965bb-6658-4416-a587-66cb98c2f61f 34 fields · synced May 30, 2026