Fibercure— 510(k) K232076
Substantially EquivalentLumendo AG
FDA 510(k) clearance K232076 for Fibercure, Substantially Equivalent on 2023-11-02. Applicant: Lumendo AG. Device class: 2.
Clearance details
- Applicant
- Lumendo AG
- Product code
- Code QNF
- Device class
- Class 2
- Regulation
- 21 CFR 872.6070
- Advisory panel
- Dental
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Renens, CH
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