Establishment registration
NORDENT MFG., INC.
FDA establishment registration 1419489 · ELK GROVE VILLAGE, US
Key facts
| Registration number | 1419489 |
|---|---|
| Establishment name | NORDENT MFG., INC. |
| Owner/operator | NORDENT MFG., INC. |
| Owner/operator number | 1419489 |
| FEI number | 1419489 |
| Address | 610 BONNIE LANE |
| City | ELK GROVE VILLAGE |
| State | IL |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | DZI, DZN, DZP, EAX, EBR, EBW, EBZ, ECP, ECR, ECS, EEF, EFB, EFK, EFL, EGN, EGS, EHD, EIG, EIK, EIR, EIS, EIX, EIY, EJB, EJG, EJI, EKB, EKC, EKD, EKG and 38 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 1,000+ 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