Establishment registration
STALLION MEDICAL, INC.
FDA establishment registration 2031962 · SAN DIEGO, US
Key facts
| Registration number | 2031962 |
|---|---|
| Establishment name | STALLION MEDICAL, INC. |
| Owner/operator | STALLION MEDICAL, INC. |
| Owner/operator number | 9012225 |
| FEI number | 3002445546 |
| Address | 3085 Beyer Blvd Suite A-105 |
| City | SAN DIEGO |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | ERA, FHQ, FLK, FQZ, FZO, GFJ, HIT, HKM, HKN, HKO, HKY, HLF, HLH, HLJ, HLL, HLM, HLQ, HLS, HMD, HME, HMF, HMR, HMX, HNA, HNB, HNC, HND, HNF, HNG, HNH and 40 more |
| Device classes | 1, 2, U |
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