Establishment registration
GUANGZHOU WONDFO BIOTECH CO., LTD.
FDA establishment registration 3004635103 · Guangzhou Guangdong, CN
Key facts
| Registration number | 3004635103 |
|---|---|
| Establishment name | GUANGZHOU WONDFO BIOTECH CO., LTD. |
| Owner/operator | GUANGZHOU WONDFO BIOTECH CO., LTD. |
| Owner/operator number | 9064561 |
| FEI number | 3004635103 |
| Address | No.8 Lizhishan Road, Science City, Huangpu District |
| City | Guangzhou Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DHA, DIC, DIO, DIS, DJG, DKZ, GTY, JHI, JXM, JXN, KHE, LAF, LCM, LCX, LDJ, MJZ, MRS, NFT, NFV, NFW, NFY, NGA, NGE, NGG, NGL, NNI, NNK, PTG, PTH, PUX 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