K232299
- 510(k) number
- K232299
- Device name
- CeraPutty
- Applicant
- Meta Biomed Co., Ltd. KR
- Product code
- KIF — Resin, Root Canal Filling
- Decision date
- 2023-09-29
- Date received
- 2023-08-01
- 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: K232299.pdf
Official FDA record: K232299
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.