K262239
- 510(k) number
- K262239
- Device name
- Obsidian® Press Over Zirconia
- Applicant
- Prismatik Dentalcraft, Inc. CA · US
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2026-07-30
- Date received
- 2026-07-01
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K262239.pdf
Official FDA record: K262239
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.