FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇹 Austria

Implantmed Plus II & Piezomed Plus II Module

K Number: K253776 · Decision Jun 18, 2026
Classifications
1
FEI Numbers
78
Registration Numbers
78
Same Product Code
48
Applicant Total
18
Review Days
204

Basic Information

Device Name
Implantmed Plus II & Piezomed Plus II Module
K Number
K253776
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
872.4120
Medical Specialty
Dental
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
W&H Dentalwerk Buermoos GmbH
Date Received
November 26, 2025
Decision Date
June 18, 2026
Product Code
DZI
Advisory Committee
Dental
Review Advisory Committee
DE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DZI Drill, Bone, Powered

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