K262300
- 510(k) number
- K262300
- Device name
- Denture Base Resin V2
- Applicant
- Formlabs Ohio, Inc. OH · US
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2026-07-08
- Date received
- 2026-07-07
- Decision
- Substantially Equivalent
- Clearance type
- Abbreviated
- Flag
- Third-party review
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K262300.pdf
Official FDA record: K262300
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.