Implantmed Plus II & Piezomed Plus II Module
K-Number: K253776 · 2026-06-18
Device Summary
Frequently Asked Questions
What is the Implantmed Plus II & Piezomed Plus II Module?
Implantmed Plus II & Piezomed Plus II Module is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is W&H Dentalwerk Buermoos GmbH. The 510(k) number is K253776.
When did Implantmed Plus II & Piezomed Plus II Module receive FDA 510(k) clearance?
Implantmed Plus II & Piezomed Plus II Module received FDA 510(k) clearance on 2026-06-18, under 510(k) number K253776.
Who is the listed applicant for Implantmed Plus II & Piezomed Plus II Module?
The FDA 510(k) record lists W&H Dentalwerk Buermoos GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Implantmed Plus II & Piezomed Plus II Module?
The FDA product code for Implantmed Plus II & Piezomed Plus II Module is DZI.
Other records listing W&H Dentalwerk Buermoos GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: DZI)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.