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Applicator 3 20900360BK

by Pollogen Ltd

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290016586565 UDI-DI Date2 Feb 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  • Withdrawn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
Applicator 3
Generic Name
Radio-frequency skin surface treatment system applicator
Model / Reference
20900360BK
Primary DI / UDI-DI
07290016586565
FDA Product Code
GEI, NGX
GMDN Term
Radio-frequency skin surface treatment system applicator
Device Class
Class II
Regulation Number
878.4400, 890.5850
GUDID distribution status
In Commercial Distribution

Other devices from Pollogen Ltd

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Properties

  • Premarket Exempt
  • Serial Number
  • Manufacturing Date

Other properties (11)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Lot / Batch Number: No
  • Expiration Date: No