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PRO Pen Microneedling System 6883

by Dermalogica, LLC

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

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 Number00666151621305 UDI-DIDate31 Jan 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade Name
PRO Pen Microneedling System
Generic Name
Cosmetic micro-needling electronic handpiece, professional
Model / Ref / Catalog
6883
Primary DI / UDI-DI
00666151621305
510(k) Number
FDA Product Code
QAI
GMDN Term
Cosmetic micro-needling electronic handpiece, 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

  • Prescription Use
  • Lot / Batch Number
  • Manufacturing Date

Other properties (11)

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