FZE
- Product code
- FZE
- Device name
- Prosthesis, Nose, Internal
- Device class
- Class 2
- 21 CFR
- 21 CFR 878.3680
- Medical specialty
- General, Plastic Surgery
- Marketing pathway
- 510(K)
- Flag
- Implant
- 510(k) clearances (last 3 years)
- 42
510(k) clearances, last 3 years (1)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K241253 | 2024-12-12 | Cmf Medicon Surgical, Inc. | Medicon Epiplating System | FDA |
Official FDA classification page: FZE
Classification and pathway per current FDA publications. Data from openFDA (CC0).