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PRO Pen 14-Pin Microneedling Cartridge 6819

by Dermalogica, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00666151621244 UDI-DI Date31 Jan 2026ListedStatusListed GUDID: in commercial distribution

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
PRO Pen 14-Pin Microneedling Cartridge
Generic Name
Cosmetic micro-needling electronic handpiece cartridge, professional
Model / Ref / Catalog
6819
Primary DI / UDI-DI
00666151621244
510(k) Number
FDA Product Code
QAI
GMDN Term
Cosmetic micro-needling electronic handpiece cartridge, professional
Device Class
Class II
Regulation Number
878.4430
GUDID distribution status
In Commercial Distribution

Related devices

Cleared under the same submission (K243800)

Other devices from Dermalogica, LLC

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date

Other properties (9)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No