OWR
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Mesh, Surgical, Non-Absorbable, Facial Implants For Plastic Surgery
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.3300
- Medical specialty
- General, Plastic Surgery
- Flags
- Implant
- FDA definition
- For reinforcement of soft tissue where weakness exists in facial plastic surgery.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| Tisuthes e-PTFE Surgical Patch (K201153) | Shanghai Suokang Medical Implants Co., Ltd. | 2023-06-13 |
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Every clearance here is in the API, with alerts when new ones post.