Establishment registration
JONES MEDICAL INSTRUMENT CO.
FDA establishment registration 1416588 · OAK BROOK, US
Key facts
| Registration number | 1416588 |
|---|---|
| Establishment name | JONES MEDICAL INSTRUMENT CO. |
| Owner/operator | JONES MEDICAL INSTRUMENT CO. |
| Owner/operator number | 1416588 |
| FEI number | 1416588 |
| Address | 200 Windsor Dr |
| City | OAK BROOK |
| State | IL |
| Country | US |
| Establishment types | Manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BZC |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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