FDA Device Establishments · JSON-LD · Markdown
FEI 3016500342 · Complaint File Establishment per 21 CFR 820.198 Manufacture Medical Device · Status: Active
| FEI Number | 3016500342 |
|---|---|
| Owner / Operator | OpZira, Inc. (#10093974) |
| Address | 1000 Kreider Drive, STE 700, Middletown, PA, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | OUM |
| Regulation § (21 CFR) | 886.1050 |
| Proprietary names | AdaptDx; AdaptDx Pro |
Source: openFDA. Public-domain (CC0).