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Bonartic TCR 8er 552790

by Candulor AG

Bonartic TCR 8er 552790 is a Class II device made by Candulor AG, listed in FDA GUDID since 4 Oct 2016 (UDI-DI E1995527901), 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 NumberE1995527901 UDI-DI Date4 Oct 2016ListedStatusListed 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  • Withdrawn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
Bonartic TCR 8er
Generic name
Resin artificial teeth
Model / Ref / Catalog
552790
Primary DI / UDI-DI
E1995527901
FDA product code
ELM
GMDN term
Resin artificial teeth
Device class
Class II
Regulation number
872.3590
GUDID distribution status
In Commercial Distribution

Related devices

Category: Resin artificial teeth

Other devices from Candulor AG

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Properties

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