Establishment registration
BIOGENEX LABORATORIES INC.
FDA establishment registration 3008776165 · Fremont, US
Key facts
| Registration number | 3008776165 |
|---|---|
| Establishment name | BIOGENEX LABORATORIES INC. |
| Owner/operator | BIOGENEX LABORATORIES INC. |
| Owner/operator number | 2936532 |
| FEI number | 2936532 |
| Address | 48810 Kato Road,Suite 100E&200E |
| City | Fremont |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | GGH, HYF, HYJ, HYL, HYW, HYZ, HZA, HZC, HZF, HZG, HZJ, HZS, HZT, HZX, HZZ, IAB, IBG, ICH, ICL, ICQ, IDA, IEO, JCC, JTS, KEO, KEW, KEY, KKP, KPA, LEE and 6 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 10–99 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