Skip to content

Implantmed Plus II & Piezomed Plus II Module

by W&H Dentalwerk Buermoos GmbH

510(k) K253776

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 23 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK253776 Date18 Jun 2026ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 23 Oct 2026.

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
DZI
Device Class
Class II
Regulation
21 CFR Part 872.4120
Advisory Committee
Dental
FDA Decision
SESE Substantially Equivalent

Other devices from W&H Dentalwerk Buermoos GmbH

See all devices from W&H Dentalwerk Buermoos GmbH →