K231932
- 510(k) number
- K231932
- Device name
- TDS (TECHWIN DENTAL SYSTEM)
- Applicant
- Techwin Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-08-20
- Date received
- 2023-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K231932.pdf
Official FDA record: K231932
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.