Establishment registration
Proactive Medical Products
FDA establishment registration 3009327812 · Mount Vernon, US
Key facts
| Registration number | 3009327812 |
|---|---|
| Establishment name | Proactive Medical Products |
| Owner/operator | PROACTIVE MEDICAL PRODUCTS LLC |
| Owner/operator number | 10039097 |
| FEI number | 3009327812 |
| Address | 590 Franklin Ave |
| City | Mount Vernon |
| State | NY |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CAF, CAN, CAW, DQA, DXN, FLL, FMP, FMR, FMW, FNG, FNJ, FNL, FNM, FOX, FSA, IKY, ILS, IML, IMM, IMP, IMR, INW, IOR, IPR, IPS, IPY, ITJ, KHA, KIC, KMI and 4 more |
| 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