Establishment registration
AIKANG MEDTECH CO., LTD
FDA establishment registration 3010402964 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3010402964 |
|---|---|
| Establishment name | AIKANG MEDTECH CO., LTD |
| Owner/operator | AIKANG MEDTECH CO., LTD |
| Owner/operator number | 10044248 |
| FEI number | 3010402964 |
| Address | 201, 3F&13F, Aikang Building 1, No.66 Juqing Rd, Jinsha Community of Kengzi, Pingshan District |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | JJC, JJI, JQC, KSE, LXG |
| 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