Establishment registration
Xeridiem Medical Devices
FDA establishment registration 2025851 · Tucson, US
Key facts
| Registration number | 2025851 |
|---|---|
| Establishment name | Xeridiem Medical Devices |
| Owner/operator | Xeridiem Medical Devices, A Spectrum Plastics Group Company |
| Owner/operator number | 2025851 |
| FEI number | 2025851 |
| Address | 4700 S Overland Dr |
| City | Tucson |
| State | AZ |
| Country | US |
| Establishment types | Repackager/relabeler, Single-use device reprocessor, Complaint file establishment |
| Registration valid through | 2026 |
| Product codes listed | BSS, EYC, GBX, IWJ, KNT, KOD, KPY, MEQ, OCM, OQY, OTK, PIF |
| Device classes | 1, 2, 3 |
At a glance
- 10–99 Device listings
- 100–999 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