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A-dec S76

by A-Dec, Inc.

A-dec S76 is a Class II device made by A-Dec, Inc., listed in FDA GUDID since 7 May 2026 (UDI-DI 10194665008857), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number10194665008857 UDI-DI Date7 May 2026ListedStatusListed GUDID: not 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  • Withdrawn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
A-dec
Generic name
Operating room light
Model / Ref / Catalog
S76
Primary DI / UDI-DI
10194665008857
FDA product code
FTD
GMDN term
Operating room light
Device class
Class II
Regulation number
878.4580
GUDID distribution status
Not in Commercial Distribution

Other devices from A-Dec, Inc.

  • A-dec 54.1073.00

    Class I
  • A-dec 54.0924.01

    Class I
  • A-dec 54.1074.01

    Class I
  • A-dec 54.1073.01

    Class I

See all devices from A-Dec, Inc. →

Properties

  • Premarket exempt
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)