FDA Device Establishments · JSON-LD · Markdown
FEI 1000139415 · Manufacture Medical Device · Status: Active
| FEI Number | 1000139415 |
|---|---|
| Owner / Operator | DMB CORPORATION (#10025785) |
| Address | 1800 JACKSON ST., SUITE 214, GOLDEN, CO, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | KYE |
| Regulation § (21 CFR) | 886.5420 |
| Proprietary names | prosthetic soft lens |
Source: openFDA. Public-domain (CC0).