K261456
- 510(k) number
- K261456
- Device name
- Ruthinium Disc
- Applicant
- Dental Manufacturing S.p.A. IT
- Product code
- POW — Crown And Bridge, Long-Term Temporary, Resin
- Decision date
- 2026-08-05
- Date received
- 2026-05-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K261456.pdf
Official FDA record: K261456
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.