Establishment registration
SHENZHEN SINO-K MEDICAL TECHNOLOGY CO., LTD.
FDA establishment registration 3015616170 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3015616170 |
|---|---|
| Establishment name | SHENZHEN SINO-K MEDICAL TECHNOLOGY CO., LTD. |
| Owner/operator | Shenzhen SINO-K Medical Technology Co., Ltd. |
| Owner/operator number | 10084033 |
| FEI number | 3015616170 |
| Address | 4th Floor, Building 2, West Side of Xixiang Veterans Industry City, Gongle Community, Xixiang Street |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DQA, DXQ, FLL, IKD |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 100–999 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