LYQ
3 FDA 510(k) clearances · Product code
FDA profile
- Official device name
- Accessories, Fixation, Spinal Intervertebral Body
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 888.4540
- Medical specialty
- Orthopedic
- Adverse events (MAUDE)
- 2006: 4
Reports received by FDA, not confirmed device causation - volume tracks device popularity as much as risk.
Export predicate table (CSV) Shareable report ◉ Watch exports: 3 free/month · reports & watching: free
| Record | Firm | Date |
|---|---|---|
| TRANS-ORAL DEPTH GAUGE (K893415) | Ruggles Corp. | 1989-06-07 |
| TSRH ANTERIOR SPINAL SCREWS, STAPLES AND END PLATE (K883784) | Warsaw Orthopedic, Inc. | 1989-04-06 |
| CASF DRILL GUIDE DG 170 (K882871) | Terray Manufacturing, Inc. | 1988-09-23 |
Track LYQ automatically
Every clearance here is in the API, with alerts when new ones post.