Establishment registration
BIALEX LAB
FDA establishment registration 3021841051 · Wichita Falls, US
Key facts
| Registration number | 3021841051 |
|---|---|
| Establishment name | BIALEX LAB |
| Owner/operator | Bialex Lab |
| Owner/operator number | 10049801 |
| FEI number | 3021841051 |
| Address | 717 Ohio Ave |
| City | Wichita Falls |
| State | TX |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | CEK, CEO, CET, CFH, CGA, CGX, CHH, CHI, CIG, CIJ, CIT, CJH, CJR, CJW, CKA, CKB, CKF, DDN, DLI, GTQ, IBA, JFJ, JGK, JGP, JGY, JII, JIT, JIY, JJG, JJX and 19 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- None 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