Establishment registration
Badger Rehab Products
FDA establishment registration 3020889880 · Mississauga Ontario, CA
Key facts
| Registration number | 3020889880 |
|---|---|
| Establishment name | Badger Rehab Products |
| Owner/operator | Badger Rehab Products |
| Owner/operator number | 10082815 |
| FEI number | 3020889880 |
| Address | 2390 Haines Rd, Unit 12 |
| City | Mississauga Ontario |
| Country | CA |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | INQ, ISA |
| Device classes | 1 |
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