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Eos Qed-4604

by Qed, Inc.

Eos Qed-4604 is a Class I device made by Qed, Inc., listed in FDA GUDID since 22 May 2025 (UDI-DI 00860013851569), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860013851569 UDI-DI Date22 May 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  • Withdrawn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
Eos
Generic name
Head-worn lamp
Model / reference
QED-4604
Primary DI / UDI-DI
00860013851569
FDA product code
HPP
GMDN term
Head-worn lamp
Device class
Class I
Regulation number
886.4335
GUDID distribution status
In Commercial Distribution

Related devices

Category: Head-worn lamp

Similar devices

Other devices filed under FDA product code HPP (Headlamp, Operating, Battery-Operated).

Other devices from Qed, Inc.

See all devices from Qed, Inc. →

Properties

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