Establishment registration
Shenzhen reanson products co.,ltd.
FDA establishment registration 3005912219 · SHENZHEN Guangdong, CN
Key facts
| Registration number | 3005912219 |
|---|---|
| Establishment name | Shenzhen reanson products co.,ltd. |
| Owner/operator | Shenzhen reanson products co.,ltd |
| Owner/operator number | 9091407 |
| FEI number | 3005912219 |
| Address | No.16, 3rd ind zone, xia village, gongming town, guangming district |
| City | SHENZHEN Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | HOY, MSH, NDA, OEA |
| Device classes | 1, 2 |
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