LZM
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Guard, Skin Graft
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4014
- Medical specialty
- General, Plastic Surgery
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| AQUAPLAST TIE DOWN DRESSING (K943871) | Wfr/Aquaplast Corp. | 1994-09-30 |
| GRAFT GUARD (K885136) | Sorex Medical | 1989-02-06 |
Track LZM automatically
Every clearance here is in the API, with alerts when new ones post.