Establishment registration
ARETE MEDICAL DEVICES
FDA establishment registration 3037007211 · Mullica Hill, US
Key facts
| Registration number | 3037007211 |
|---|---|
| Establishment name | ARETE MEDICAL DEVICES |
| Owner/operator | Arete Medical Devices |
| Owner/operator number | 10093092 |
| FEI number | 3037007211 |
| Address | 157 Bridgeton Pike STE 200-252 |
| City | Mullica Hill |
| State | NJ |
| Country | US |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | CAE |
| 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