Skip to content

Applicator 1 20900340BK

by Pollogen Ltd

Applicator 1 20900340BK is a Class II device made by Pollogen Ltd, listed in FDA GUDID since 2 Feb 2026 (UDI-DI 07290016586770), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number07290016586770 UDI-DI Date2 Feb 2026ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
Applicator 1
Generic name
Radio-frequency skin surface treatment system applicator
Model / reference
20900340BK
Primary DI / UDI-DI
07290016586770
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

Similar devices

Other devices filed under FDA product code GEI (Electrosurgical, Cutting & Coagulation & Accessories).

Other devices from Pollogen Ltd

See all devices from Pollogen Ltd →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)