Establishment registration
Devicor Medical Products, Inc. Warehouse/Distribution/Service Center
FDA establishment registration 3010339638 · Blue Ash, US
Key facts
| Registration number | 3010339638 |
|---|---|
| Establishment name | Devicor Medical Products, Inc. Warehouse/Distribution/Service Center |
| Owner/operator | Devicor Medical Products, Inc. |
| Owner/operator number | 10033297 |
| FEI number | 3010339638 |
| Address | 4750 Lake Forest Dr Ste 120 |
| City | Blue Ash |
| State | OH |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | KNW, NEU |
| Device classes | 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