Glidewell 3DP Denture Base Resin— 510(k) K241493
Substantially EquivalentPrismatik Dentalcraft, Inc.
FDA 510(k) clearance K241493 for Glidewell 3DP Denture Base Resin, Substantially Equivalent on 2024-09-12. Applicant: Prismatik Dentalcraft, Inc..
Clearance details
- Applicant
- Prismatik Dentalcraft, Inc.
- Product code
- Code EBI
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Adverse events under product code EBI
product code EBI- Other
- 1
- Total
- 1
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.