Establishment registration
WILTROM INC.
FDA establishment registration 3014387294 · San Jose, US
Key facts
| Registration number | 3014387294 |
|---|---|
| Establishment name | WILTROM INC. |
| Owner/operator | Wiltrom Inc. |
| Owner/operator number | 10059962 |
| FEI number | 3014387294 |
| Address | 2880 Zanker Road, Suite 103 |
| City | San Jose |
| State | CA |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | LXH, MQV, NKB |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 100–999 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