K253324
- 510(k) number
- K253324
- Device name
- UltraPrint-Dental Denture UV
- Applicant
- Guangzhou Heygears IMC., Inc. CN
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2025-11-20
- Date received
- 2025-09-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K253324.pdf
Official FDA record: K253324
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.