FTQ
2 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Prosthesis, Penis, Rigid Rod
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 876.3630
- Medical specialty
- Gastroenterology, Urology
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| VIRILIS PENILE PROSTHESIS (K983015) | Specialty Surgical Products, Inc. | 1999-02-05 |
| SILICONE-SILVER PENILE PROSTHESIS-ESK (K830667) | Dacomed Corp. | 1983-10-20 |
Track FTQ automatically
Every clearance here is in the API, with alerts when new ones post.