FDA Device Establishments · JSON-LD · Markdown
FEI 3009026057 · Manufacture Medical Device · Status: Active
| FEI Number | 3009026057 |
|---|---|
| Owner / Operator | LENSAR, Inc (#10041040) |
| Address | 2800 Discovery Drive, Suite 100, Orlando, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OOE |
| Regulation § (21 CFR) | 886.4390 |
| Proprietary names | ALLY Adaptive Cataract Treatment System |
Source: openFDA. Public-domain (CC0).