FXG
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Specula Accessories
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 878.1800
- 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.
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| Record | Firm | Date | Builder |
|---|---|---|---|
| 3MM DISPOSABLE SPECULA (K891589) | Semantodontics, Inc. | 1989-04-18 | + Add |
Track FXG automatically
Every clearance here is in the API, with alerts when new ones post.