K261802
- 510(k) number
- K261802
- Device name
- Glidewell Denture Base Resin
- Applicant
- Prismatik Dentalcraft, Inc. CA · US
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2026-08-27
- Date received
- 2026-06-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K261802.pdf
Official FDA record: K261802
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.