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Batrik Bitestron Bite Blocks B3

by Batrik Medical Manufacturing Inc

Batrik Bitestron Bite Blocks B3 is a Class I device made by Batrik Medical Manufacturing Inc, listed in FDA GUDID since 25 Sep 2020 (UDI-DI 00690521000254), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00690521000254 UDI-DI Date25 Sep 2020ListedStatusListed 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  • Withdrawn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
Batrik Bitestron Bite Blocks
Generic name
Endoscopic bite block, basic, single-use
Model / Ref / Catalog
B3
Description
Bitestrong Bite Blocks, with strap, 20 mm, Adult, single use
Primary DI / UDI-DI
00690521000254
FDA product code
MNK
GMDN term
Endoscopic bite block, basic, single-use
Device class
Class I
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Endoscopic bite block, basic, single-use

Similar devices in this category

Other devices filed under Endoscopic bite block, basic, single-use.

Other devices from Batrik Medical Manufacturing Inc.

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Properties

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