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Edenta K900445-1000

by Edenta Etablissement

Edenta K900445-1000 is a Class I device made by Edenta Etablissement, listed in FDA GUDID since 3 Feb 2022 (UDI-DI E312K90044510001), 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 NumberE312K90044510001 UDI-DI Date3 Feb 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  • Withdrawn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
Edenta
Generic name
Dental restoration retention pin
Model / reference
K900445-1000
Primary DI / UDI-DI
E312K90044510001
FDA product code
EBL
GMDN term
Dental restoration retention pin
Device class
Class I
Regulation number
872.3740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Dental restoration retention pin

Other devices from Edenta Etablissement

See all devices from Edenta Etablissement →

Properties

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