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Conair FB5X

by Conair LLC.

Conair FB5X is a Class I device made by Conair LLC., listed in FDA GUDID since 25 Apr 2022 (UDI-DI 00074108226495), 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 Number00074108226495 UDI-DI Date25 Apr 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  • Withdrawn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
Foot bath
Model / reference
FB5X
Primary DI / UDI-DI
00074108226495
FDA product code
ISA
GMDN term
Foot bath
Device class
Class I
Regulation number
890.5660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Foot bath

Other devices from Conair LLC.

See all devices from Conair LLC. →

Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)