K243478
- 510(k) number
- K243478
- Device name
- Straumann InLab Validated Workflow
- Applicant
- Institut Straumann AG CH
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2025-02-19
- Date received
- 2024-11-08
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.6 MB · U.S. public domain
Also available from FDA: K243478.pdf
Official FDA record: K243478
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.