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McKesson 16-429

by Mckesson Medical-Surgical Inc.

McKesson 16-429 is an endoscopic bite block (FDA Class I; FDA product code MNK, Endoscopic Bite Block) made by Mckesson Medical-Surgical Inc., listed in FDA GUDID since 31 Aug 2022 (UDI-DI 20612479186044), 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 Number20612479186044 UDI-DI Date31 Aug 2022ListedStatusListed GUDID: 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  • Withdrawn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
McKesson
Generic name
Endoscopic bite block, basic, reusable
Model / reference
16-429
Primary DI / UDI-DI
20612479186044
FDA product code
MNK
GMDN term
Endoscopic bite block, basic, reusable
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, reusable

Other devices from Mckesson Medical-Surgical Inc.

See all devices from Mckesson Medical-Surgical Inc. →

Properties

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