FDA Device Establishments · JSON-LD · Markdown
FEI 3016804805 · Manufacture Medical Device Complaint File Establishment per 21 CFR 820.198 Develop Specifications But Do Not Manufacture At This Facility · Status: Active
| FEI Number | 3016804805 |
|---|---|
| Owner / Operator | ClearCam (#10072510) |
| Address | 8000 Centre Park Dr, 170, Austin, TX, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | GCJ |
| Regulation § (21 CFR) | 876.1500 |
| Proprietary names | ClearScope; ClearCam Kelling System; ClearCam System; Kelling |
Source: openFDA. Public-domain (CC0).