LNX
1 FDA 510(k) clearances · Product code
FDA profile
- Adverse events (MAUDE)
- 2015: 18 · 2016: 14 · 2020: 13 · 2021: 20 · 2022: 18 · 2023: 15
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 |
|---|---|---|
| OCEANIA HEALTH CARE SYSTEMS ELECTRONIC MEDICAL REC (K921846) | Oceania Health Care Systems, Inc. | 1994-08-08 |
Track LNX automatically
Every clearance here is in the API, with alerts when new ones post.