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Bite fork 662451

by Candulor AG

Bite fork 662451 is a Class I device made by Candulor AG, listed in FDA GUDID since 16 Nov 2023 (UDI-DI E1996624511), 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 NumberE1996624511 UDI-DI Date16 Nov 2023ListedStatusListed 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  • Withdrawn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 fork
Generic name
Dental articulator
Model / Ref / Catalog
662451
Primary DI / UDI-DI
E1996624511
FDA product code
KCR
GMDN term
Dental articulator
Device class
Class I
Regulation number
872.3220
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Dental articulator

Similar devices

Other devices filed under FDA product code KCR (FACEBOW).

Other devices from Candulor AG

See all devices from Candulor AG →

Properties

  • Sterilise before use
  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (9, all answered No)