Establishment registration
SHENZHEN DENCO MEDICAL CO., LTD.
FDA establishment registration 3011554142 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3011554142 |
|---|---|
| Establishment name | SHENZHEN DENCO MEDICAL CO., LTD. |
| Owner/operator | SHENZHEN DENCO MEDICAL CO., LTD. |
| Owner/operator number | 10048487 |
| FEI number | 3011554142 |
| Address | Rm 3108, Bldg 6, Tian'an Cloud Park, Bantian Str, Longgang Dist, |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DZA, DZC, DZD, DZM, DZN, DZP, EAX, EAZ, EBL, EBR, ECI, ECM, ECO, ECP, EFL, EGD, EGZ, EHK, EHM, EHY, EHZ, EIB, EID, EIE, EIF, EIL, EIY, EJB, EJF, EJL and 22 more |
| Device classes | 1, 2 |
At a glance
- 10–99 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