Establishment registration
CAMBER SPINE TECHNOLOGIES
FDA establishment registration 3010197239 · King of Prussia, US
Key facts
| Registration number | 3010197239 |
|---|---|
| Establishment name | CAMBER SPINE TECHNOLOGIES |
| Owner/operator | Camber Spine/Medical Technologies |
| Owner/operator number | 10043961 |
| FEI number | 3010197239 |
| Address | 501 Allendale Rd |
| City | King of Prussia |
| State | PA |
| Country | US |
| Establishment types | Export-only manufacturer |
| Registration valid through | 2026 |
| Product codes listed | FMF, FSM, FZO, FZX, FZY, GAD, GDM, HTF, HTJ, HTR, HTW, HTX, HWJ, HWX, HXB, HXG, HXL, HXX, JAC, KQM, KTZ, KWQ, LXH, MAX, MNH, MNI, MQP, MQV, NKB, ODP and 4 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