Establishment registration
RESPONSIVE ARTHROSCOPY
FDA establishment registration 3015200759 · Minneapolis, US
Key facts
| Registration number | 3015200759 |
|---|---|
| Establishment name | RESPONSIVE ARTHROSCOPY |
| Owner/operator | Responsive Arthroscopy |
| Owner/operator number | 10059367 |
| FEI number | 3015200759 |
| Address | 701 N 3rd Street, Suite 208 |
| City | Minneapolis |
| State | MN |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | FSM, GFG, HWC, JDR, LXH, MBI |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 100–999 UDI devices (GUDID)
- Current Registration current
- 1–9 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