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Bite Wing Loops 6070553344

by Maxill, Inc.

Bite Wing Loops 6070553344 is a Class I device made by Maxill, Inc., listed in FDA GUDID since 22 Jul 2022 (UDI-DI D89260705533441), 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 NumberD89260705533441 UDI-DI Date22 Jul 2022ListedStatusListed 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  • Withdrawn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
Bite Wing Loops
Generic name
Dental x-ray film holder, single-use
Model / reference
6070553344
Primary DI / UDI-DI
D89260705533441
FDA product code
NRD
GMDN term
Dental x-ray film holder, single-use
Device class
Class I
Regulation number
872.6640
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental x-ray film holder, single-use

Other devices from Maxill, Inc.

See all devices from Maxill, Inc. →

Properties

  • Single use
  • Premarket exempt
Other properties (13, all answered No)