Establishment registration
US PATIENTCARE PRODUCTS LLC
FDA establishment registration 3026400153 · Bixby, US
Key facts
| Registration number | 3026400153 |
|---|---|
| Establishment name | US PATIENTCARE PRODUCTS LLC |
| Owner/operator | US PATIENTCARE PRODUCTS LLC |
| Owner/operator number | 10087359 |
| FEI number | 3026400153 |
| Address | 12139 South Sheridan Road |
| City | Bixby |
| State | OK |
| Country | US |
| Establishment types | Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | KMI, PJO, PJP |
| 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