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Diamodent B500

by Diamodent

Diamodent B500 is a Class II device made by Diamodent, cleared under FDA 510(k) K010619 on 28 Sep 2001 and listed in FDA GUDID since 4 Jan 2019 (UDI-DI D907B5000), active as of 22 Oct 2026.

Active United States. Also listed in GUDID (US).

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K010619

FDA submission, from GUDID

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberD907B5000 UDI-DI Date4 Jan 2019ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE from GUDID Substantially Equivalent · Traditional NumberK010619 Date28 Sep 2001DecidedStatusActive

Official records

Across registries

2 registries list this device

  • FDA 510(k) K010619 decided 28 Sep 2001 Active
  • FDA GUDID UDI-DI D907B5000 listed 4 Jan 2019 Listed

Timeline

2 dated events

  1. Cleared FDA 510(k) K010619
  2. Listed FDA GUDID D907B5000

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

GUDID

Trade name
Diamodent
Generic name
Dental implant suprastructure, permanent, preformed
Description
Compatible with: 5.0 Wide Platform (WP) Branemark implants Cement-On Post, Titanium 1.4mm Collar, 6mm Profile
Catalogue number
B500
Primary DI / UDI-DI
D907B5000
510(k) Number
FDA product code
DZE
GMDN term
Dental implant suprastructure, permanent, preformed
Device class
Class II
Regulation number
872.3640
GUDID distribution status
In Commercial Distribution
Sterilisation method
Dry Heat Sterilization

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Properties

  • Sterilise before use
  • Implantable
  • Prescription use
  • Lot / batch number
Other properties (11, all answered No)