Establishment registration
Crosstex International
FDA establishment registration 1319130 · Rush, US
Key facts
| Registration number | 1319130 |
|---|---|
| Establishment name | Crosstex International |
| Owner/operator | SPS/Crosstex International |
| Owner/operator number | 1319130 |
| FEI number | 1319130 |
| Address | 6789 WEST HENRIETTA RD. |
| City | Rush |
| State | NY |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DYN, ECB, EFA, EFH, EFN, EGS, EGZ, EHZ, EIA, EIE, EJR, EKF, FLG, FMA, FRC, FRG, FXX, FYE, JOJ, JRG, KCT, KHR, KME, KMT, KXF, KYW, LBH, LRJ, MED, MSH and 3 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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