AincA® AP-374-3

by Anesthesia Associates, Inc.

AincA® AP-374-3 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005AP37430), 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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	NumberB005AP37430 UDI-DI	Date31 Mar 2021Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

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Withdrawn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: AP-374-3

Primary DI / UDI-DI: B005AP37430
FDA product code: CCW
GMDN term: Rigid intubation laryngoscope, reusable

Device class: Class I
Regulation number: 868.5540
GUDID distribution status: In Commercial Distribution

Other devices from Anesthesia Associates, Inc.

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Class I
AincA 00-488

Class II
AincA® AP-374-4

Class I
AincA® 00-100-PLUS

Class II

See all devices from Anesthesia Associates, Inc. →

Properties

Prescription use
Premarket exempt
Lot / batch number

Other properties (12, all answered No)