Establishment registration
AMPLIO SPINE
FDA establishment registration 3047379549 · Boca Raton, US
Key facts
| Registration number | 3047379549 |
|---|---|
| Establishment name | AMPLIO SPINE |
| Owner/operator | Amplio Spine |
| Owner/operator number | 10096118 |
| FEI number | 3047379549 |
| Address | 1060 Holland Drive, Suite G |
| City | Boca Raton |
| State | FL |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | PEK |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 10–99 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