Establishment registration
EKSO BIONICS
FDA establishment registration 3009495988 · San Rafael, US
Key facts
| Registration number | 3009495988 |
|---|---|
| Establishment name | EKSO BIONICS |
| Owner/operator | Ekso Bionics |
| Owner/operator number | 10050306 |
| FEI number | 3009495988 |
| Address | 101 Glacier Point |
| City | San Rafael |
| State | CA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | IOD, IOL, IQI, ITJ, PHL |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 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