ScanX Edge— 510(k) K202633
Substantially EquivalentDürr Dental SE
FDA 510(k) clearance K202633 for ScanX Edge, Substantially Equivalent on 2020-10-07. Applicant: Dürr Dental SE. Device class: 2.
Clearance details
- Applicant
- Dürr Dental SE
- Product code
- Code MUH
- Device class
- Class 2
- Regulation
- 21 CFR 872.1800
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Bietigheim-Bissingen, DE
Recent devices under product code MUH
view allMore clearances from Dürr Dental SE
view allData sourced from openFDA. This site is unofficial and independent of the FDA.