FDA Device Establishments · JSON-LD · Markdown
FEI 1000306694 · Develop Specifications But Do Not Manufacture At This Facility Manufacture Medical Device for Another Party (Contract Manufacturer) Manufacture Medical Device Repack or Relabel Medical Device · Status: Active
| FEI Number | 1000306694 |
|---|---|
| Owner / Operator | Tecomet (#10031318) |
| Address | 5307 95th Ave, KENOSHA, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | EMH |
| Regulation § (21 CFR) | 872.4565 |
Source: openFDA. Public-domain (CC0).