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DiamoDent AJ801

by Diamodent

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD907AJ8010 UDI-DI Date14 Apr 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  • Withdrawn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
DiamoDent
Generic name
Dental implant suprastructure, temporary, preformed, reusable
Description
TEMPORARY ABUTMENT, Non-Hexed 1.0mm Collar, 4.2mm Profile 3.4mm, BIOMET 3i, Certain Implants
Catalogue number
AJ801
Primary DI / UDI-DI
D907AJ8010
FDA product code
NHA
GMDN term
Dental implant suprastructure, temporary, preformed, reusable
Device class
Class II
Regulation number
872.3630
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization

Related devices

Category: Dental implant suprastructure, temporary, preformed, reusable

Other devices from Diamodent

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Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number

Other properties (10)

  • Supplied sterile: No
  • Contains latex: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Premarket exempt: No
  • Serial number: No
  • Expiration date: No
  • Manufacturing date: No