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Conair Fbem

by Conair LLC.

Conair Fbem is a Class I device made by Conair LLC., listed in FDA GUDID since 28 Jul 2022 (UDI-DI 00074108356703), 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 Number00074108356703 UDI-DI Date28 Jul 2022ListedStatusListed 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  • Withdrawn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
Conair
Generic name
Dermabrasion brush, rotary
Model / reference
FBEM
Primary DI / UDI-DI
00074108356703
FDA product code
GFE
GMDN term
Dermabrasion brush, rotary
Device class
Class I
Regulation number
878.4820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dermabrasion brush, rotary

Similar devices

Other devices filed under FDA product code GFE (Brush, Dermabrasion, Powered).

Other devices from Conair LLC.

See all devices from Conair LLC. →

Properties

  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)