Establishment registration
LAKONG MEDICAL DEVICES CO., LTD.
FDA establishment registration 3008559238 · Dongguan Guangdong, CN
Key facts
| Registration number | 3008559238 |
|---|---|
| Establishment name | LAKONG MEDICAL DEVICES CO., LTD. |
| Owner/operator | Lakong Medical Devices Co., Ltd. |
| Owner/operator number | 10033552 |
| FEI number | 3008559238 |
| Address | No. 13 Jingci Road |
| City | Dongguan Guangdong |
| Country | CN |
| Establishment types | Repackager/relabeler, Remanufacturer |
| Registration valid through | 2026 |
| Product codes listed | BRY, BTI, DZA, EAY, EAZ, EBR, ECB, EFD, EFN, EGZ, EHK, EHZ, EIA, EID, EJR, ELA, ELC, EMN, FLG, FLL, FRG, FSM, FZK, FZM, HOY, IXC, JER, JOJ, KLC, KMT and 12 more |
| Device classes | 1, 2, N |
At a glance
- 10–99 Device listings
- 10–99 UDI devices (GUDID)
- Current Registration current
- 1–9 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