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AincA® 00-199-TOP

by Anesthesia Associates, Inc.

AincA® 00-199-TOP is a Class II device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B00500199TOP0), 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 NumberB00500199TOP0 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  • Withdrawn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
Airway pressure monitor, non-powered
Model / Ref / Catalog
00-199-TOP
Primary DI / UDI-DI
B00500199TOP0
FDA product code
CAP
GMDN term
Airway pressure monitor, non-powered
Device class
Class II
Regulation number
868.2600
GUDID distribution status
In Commercial Distribution

Related devices

Category: Airway pressure monitor, non-powered

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Other devices filed under Airway pressure monitor, non-powered.

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Properties

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