Establishment registration
LUMIQUICK DIAGNOSTICS, INC.
FDA establishment registration 3005984081 · SANTA CLARA, US
Key facts
| Registration number | 3005984081 |
|---|---|
| Establishment name | LUMIQUICK DIAGNOSTICS, INC. |
| Owner/operator | LUMIQUICK DIAGNOSTICS, INC. |
| Owner/operator number | 9093981 |
| FEI number | 3005984081 |
| Address | 2946 SCOTT BLVD. |
| City | SANTA CLARA |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CDP, CDZ, CEP, CFT, CGJ, DBF, DCK, DGC, DIO, DIS, DJC, DJG, DJR, DKX, DKZ, DMJ, DNK, DPN, DRR, ETA, GNC, GOD, GTY, JHI, JLB, JLW, JXM, JXN, JZG, KHE and 29 more |
| Device classes | 1, 2, N, U |
At a glance
- 10–99 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