The FDA cleared Implantmed Plus II & Piezomed Plus II Module, a powered bone drill from W&H Dentalwerk Buermoos GmbH (Buermoos, AT), under 510(k) K253776 on June 18, 2026.
- Source
- U.S. FDA 510(k) database
accessdata.fda.gov - Published
- June 18, 2026
- Type
- FDA
- Checked
- October 2, 2026
