Establishment registration
GuoLong (Shenzhen) High Technology Co., Ltd
FDA establishment registration 3009746042 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3009746042 |
|---|---|
| Establishment name | GuoLong (Shenzhen) High Technology Co., Ltd |
| Owner/operator | GuoLong (Shenzhen) High Technology Co., Ltd. |
| Owner/operator number | 10041463 |
| FEI number | 3009746042 |
| Address | Floor 1 Bldg E Dehuida Ind Park No. 237 |
| City | Shenzhen Guangdong |
| Country | CN |
| Establishment types | Specification developer, Repackager/relabeler |
| Registration valid through | 2026 |
| Product codes listed | GWI, IKW, ILD, ILH, IRO, ITC, KQW, LYG, OHY |
| Device classes | 1 |
At a glance
- 1–9 Device listings
- None 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