Establishment registration
STEPHENS INSTRUMENTS, INC
FDA establishment registration 1045379 · LEXINGTON, US
Key facts
| Registration number | 1045379 |
|---|---|
| Establishment name | STEPHENS INSTRUMENTS, INC |
| Owner/operator | STEPHENS INSTRUMENTS, INC. |
| Owner/operator number | 1045379 |
| FEI number | 1045379 |
| Address | 2500 Sandersville Rd |
| City | LEXINGTON |
| State | KY |
| Country | US |
| Establishment types | Contract manufacturer, Specification developer |
| Registration valid through | 2026 |
| Product codes listed | ECB, FHQ, FMH, FSM, GDI, GDM, GDZ, HJB, HJF, HKR, HLE, HLN, HMQ, HMR, HMX, HMZ, HNA, HNB, HNC, HND, HNF, HNG, HNH, HNI, HNJ, HNK, HNL, HNN, HNQ, HNR and 23 more |
| Device classes | 1, 2, U |
At a glance
- 10–99 Device listings
- 10–99 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