Skip to content

Fielmann COMFORT 084 FLEX CL_60090

by Fielmann Group AG

Fielmann COMFORT 084 FLEX CL_60090 is a Class I device made by Fielmann Group AG, listed in FDA GUDID since 19 Dec 2025 (UDI-DI 04066209012035), 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 Number04066209012035 UDI-DI Date19 Dec 2025ListedStatusListed 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  • Withdrawn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
Fielmann
Generic name
Spectacle frame
Model / reference
COMFORT 084 FLEX CL_60090
Primary DI / UDI-DI
04066209012035
FDA product code
HQZ
GMDN term
Spectacle frame
Device class
Class I
Regulation number
886.5842
GUDID distribution status
In Commercial Distribution

Other devices from Fielmann Group AG

See all devices from Fielmann Group AG →

Properties

  • Premarket exempt
Other properties (14, all answered No)