Establishment registration
WONDFO USA CO., LTD.
FDA establishment registration 3007606081 · Bolingbrook, US
Key facts
| Registration number | 3007606081 |
|---|---|
| Establishment name | WONDFO USA CO., LTD. |
| Owner/operator | Wondfo USA Co., Ltd. |
| Owner/operator number | 10028951 |
| FEI number | 3007606081 |
| Address | 890 Remington Blvd |
| City | Bolingbrook |
| State | IL |
| Country | US |
| Registration valid through | 2026 |
| Product codes listed | DHA, DIC, DIO, DIS, DJG, DKZ, GTY, JHI, JXM, JXN, KHE, KHO, LAF, LCM, LCX, LDJ, MJZ, MRS, NFT, NFV, NFW, NFY, NGA, NGE, NGG, NGL, NNI, NNK, PTG, PTH and 14 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