LQS
1 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Spermatocele, Alloplastic
- Device class
- Unclassified
- Medical specialty
- Unknown
- Flags
- Implant
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| MENTOR ALLOPLASTIC SPERMATOCELE (K863565) | Mentor Corp. | 1986-11-19 |
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Every clearance here is in the API, with alerts when new ones post.