KDA
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Prosthesis, Ptfe/Carbon-Fiber
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 878.3500
- Medical specialty
- General, Plastic Surgery
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MEDCARE SUTURE SCISSORS (SUTURE/GAUZE WEIGHT) (K861806) | Medcomp Technologies, Inc. | 1986-05-23 |
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Every clearance here is in the API, with alerts when new ones post.