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AincA® GL-361-0

by Anesthesia Associates, Inc.

AincA® GL-361-0 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005GL36100), 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 NumberB005GL36100 UDI-DI Date31 Mar 2021ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
AincA®
Generic name
Rigid intubation laryngoscope, reusable
Model / Ref / Catalog
GL-361-0
Primary DI / UDI-DI
B005GL36100
FDA product code
CCW
GMDN term
Rigid intubation laryngoscope, reusable
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid intubation laryngoscope, reusable

Other devices from Anesthesia Associates, Inc.

See all devices from Anesthesia Associates, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)