Establishment registration
EPITOPE DIAGNOSTICS, INC.
FDA establishment registration 2032839 · SAN DIEGO, US
Key facts
| Registration number | 2032839 |
|---|---|
| Establishment name | EPITOPE DIAGNOSTICS, INC. |
| Owner/operator | EPITOPE DIAGNOSTICS, INC. |
| Owner/operator number | 9059077 |
| FEI number | 3004185580 |
| Address | 17034 Camino San Bernardo |
| City | SAN DIEGO |
| State | CA |
| Country | US |
| Establishment types | Specification developer |
| Registration valid through | 2026 |
| Product codes listed | CDD, CDP, CDX, CDZ, CEC, CEP, CEW, CFL, CFP, CFT, CGC, CGJ, CGN, CHP, CKG, DAD, DAJ, DBF, DDR, DEG, DHA, DHX, GHH, GOD, JJE, JKD, JKR, JLB, JLS, JLW and 47 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- None 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