Establishment registration
Diagnostic Automation/ Cortez Diagnostics Inc,.
FDA establishment registration 2029372 · Woodland Hills, US
Key facts
| Registration number | 2029372 |
|---|---|
| Establishment name | Diagnostic Automation/ Cortez Diagnostics Inc,. |
| Owner/operator | Diagnostic Automation /Cortez Diagnostics Inc. |
| Owner/operator number | 9011974 |
| FEI number | 1000306617 |
| Address | 21250 Califa St Suite 102 and 116 |
| City | Woodland Hills |
| State | CA |
| Country | US |
| Establishment types | Remanufacturer |
| Registration valid through | 2026 |
| Product codes listed | CDM, CDP, CDZ, CEC, CEE, CEN, CEP, CFL, CFP, CFT, CGA, CGF, CGI, CGJ, CHP, CIZ, DAM, DAP, DBE, DBF, DBL, DBM, DCK, DCN, DDC, DDN, DEL, DFC, DFJ, DHC and 163 more |
| Device classes | 1, 2, 3, N, U |
At a glance
- 100–999 Device listings
- 1,000+ 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