FTX
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Mirror, General & Plastic Surgery
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.4800
- Medical specialty
- General, Plastic Surgery
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Both buttons carry the same predicate table: the CSV downloads for your worksheet, the report is a shareable page for clients. Exports: 3 free/month with an account · reports & watching free.
Building a predicate table? Click + Add on candidates below (up to 8), then compare and export from your Builder.
| Record | Firm | Date | Builder |
|---|---|---|---|
| REFLECTIVE MIRROR/CO2 LASER SURG CAT. #902002-000 (K870790) | Lifestream Int'L, Inc. | 1987-04-01 | + Add |
Track FTX automatically
Every clearance here is in the API, with alerts when new ones post.