Establishment registration
SUREAX MEDICAL, CORPORATION
FDA establishment registration 3024682301 · San Diego, US
Key facts
| Registration number | 3024682301 |
|---|---|
| Establishment name | SUREAX MEDICAL, CORPORATION |
| Owner/operator | SureAx Medical, Corporation |
| Owner/operator number | 10086251 |
| FEI number | 3024682301 |
| Address | 11107 Roselle St 237 |
| City | San Diego |
| State | CA |
| Country | US |
| Establishment types | Specification developer, Single-use device reprocessor |
| Registration valid through | 2026 |
| Product codes listed | DQX, GAA, GDF |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- None 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