K243094
- 510(k) number
- K243094
- Device name
- Quickdent Dental Implant System
- Applicant
- Quickdent Devices Private , Ltd. IN
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-12-19
- Date received
- 2024-09-30
- 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: K243094.pdf
Official FDA record: K243094
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.