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AincA® 00-486

by Anesthesia Associates, Inc.

AincA® 00-486 is a Class I device made by Anesthesia Associates, Inc., listed in FDA GUDID since 31 Mar 2021 (UDI-DI B005004863), 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 NumberB005004863 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  • Withdrawn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
Oropharyngeal airway, single-use
Model / Ref / Catalog
00-486
Primary DI / UDI-DI
B005004863
FDA product code
CAE
GMDN term
Oropharyngeal airway, single-use
Device class
Class I
Regulation number
868.5110
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe
Size
Length — 10 Centimeter

Related devices

Category: Oropharyngeal airway, single-use

Other devices from Anesthesia Associates, Inc.

See all devices from Anesthesia Associates, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)