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FAQ LED Panel Black

by Foreo Inc

FAQ LED Panel Black is a Class II device made by Foreo Inc, listed in FDA GUDID since 2 Mar 2026 (UDI-DI 07640260120600), 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 Number07640260120600 UDI-DI Date2 Mar 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  • Withdrawn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
FAQ LED Panel
Generic name
Blue/red/infrared phototherapy lamp
Model / reference
Black
Primary DI / UDI-DI
07640260120600
FDA product code
OHS, OLP
GMDN term
Blue/red/infrared phototherapy lamp
Device class
Class II
Regulation number
878.4810
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code OHS (Light Based Over The Counter Wrinkle Reduction).

Other devices from Foreo Inc

See all devices from Foreo Inc →

Properties

  • Over-the-counter
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)