FDA Device Establishments · JSON-LD · Markdown
FEI 3042641209 · Repack or Relabel Medical Device · Status: Active
| FEI Number | 3042641209 |
|---|---|
| Owner / Operator | ANGELALIGN MANUFACTURING CORP. (#10094928) |
| Address | 10551 S Oakview Pkwy, Oak Creek, WI, US |
| Registration expiry | 2026 |
| Initial importer flag | N |
| Registered products | 1 |
| Product codes (top 20) | DYT |
| Regulation § (21 CFR) | 872.5525 |
Source: openFDA. Public-domain (CC0).