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TRAB(TM)360 Trabeculotomy System FG 03706

by Sight Sciences, Inc.

TRAB(TM)360 Trabeculotomy System FG 03706 is a Class I device made by Sight Sciences, Inc., listed in FDA GUDID since 23 Nov 2016 (UDI-DI 00858027006112), not in commercial distribution (GUDID) as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00858027006112 UDI-DI Date23 Nov 2016ListedStatusListed 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  • Withdrawn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
TRAB(TM)360 Trabeculotomy System
Generic name
Trabeculotome, single-use
Model / reference
FG 03706
Primary DI / UDI-DI
00858027006112
FDA product code
HMZ
GMDN term
Trabeculotome, single-use
Device class
Class I
Regulation number
886.4350
GUDID distribution status
Not in Commercial Distribution

Other devices from Sight Sciences, Inc.

See all devices from Sight Sciences, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)