Establishment registration
OSTEOMED
FDA establishment registration 2027754 · ADDISON, US
Key facts
| Registration number | 2027754 |
|---|---|
| Establishment name | OSTEOMED |
| Owner/operator | OSTEOMED |
| Owner/operator number | 9000613 |
| FEI number | 2027754 |
| Address | 3885 Arapaho Rd |
| City | ADDISON |
| State | TX |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | DZE, DZJ, DZL, EFB, EJL, FMF, FSM, FZX, FZY, GAC, GDJ, GFA, GFF, GWO, GXN, GXR, HAE, HAO, HBE, HRS, HTD, HTE, HTF, HTJ, HTN, HTO, HTP, HTQ, HTW, HWA and 29 more |
| Device classes | 1, 2, U |
At a glance
- 100–999 Device listings
- 1,000+ UDI devices (GUDID)
- Current Registration current
- 10–99 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