Establishment registration
ANGELALIGN MANUFACTURING CORP.
FDA establishment registration 3042641209 · Oak Creek, US
Key facts
| Registration number | 3042641209 |
|---|---|
| Establishment name | ANGELALIGN MANUFACTURING CORP. |
| Owner/operator | ANGELALIGN MANUFACTURING CORP. |
| Owner/operator number | 10094928 |
| FEI number | 3042641209 |
| Address | 10551 S Oakview Pkwy |
| City | Oak Creek |
| State | WI |
| Country | US |
| Establishment types | Contract manufacturer, Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | DYT, NXC |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- None UDI devices (GUDID)
- Current Registration current
- None FDA inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device establishment registrations
Device establishments that manufacture, repackage, relabel or import devices for the U.S. market must register annually with the FDA and list the devices they produce.
Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database