FDA Device Establishments · JSON-LD · Markdown
FEI 3030057595 · Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3030057595 |
|---|---|
| Owner / Operator | Lombart Instrument, Inc d/b/a Advancing Eyecare (#10092771) |
| Address | 11825 Central Pkwy, Jacksonville, FL, US |
| Registration expiry | 2026 |
| Initial importer flag | Y |
| Registered products | 1 |
| Product codes (top 20) | HLM |
| Regulation § (21 CFR) | 886.1425 |
| Proprietary names | Digital Phoropter DR900; Auto Lensmeter DL2000S; Auto Ref/K K900 |
Source: openFDA. Public-domain (CC0).