Establishment registration
SHANGHAI TKLEAN MEDTECH CO., LTD.
FDA establishment registration 3024064703 · Shanghai, CN
Key facts
| Registration number | 3024064703 |
|---|---|
| Establishment name | SHANGHAI TKLEAN MEDTECH CO., LTD. |
| Owner/operator | Shanghai Tklean Medtech CO., LTD. |
| Owner/operator number | 10089286 |
| FEI number | 3024064703 |
| Address | Room 368, Sector 302, No. 211 North Fute Road, Shanghai Pilot Free Trade Zone |
| City | Shanghai |
| Country | CN |
| Establishment types | Foreign exporter |
| Registration valid through | 2026 |
| Product codes listed | FLG |
| 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