Establishment registration
SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY
FDA establishment registration 3004992978 · SHANGHAI, CN
Key facts
| Registration number | 3004992978 |
|---|---|
| Establishment name | SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY |
| Owner/operator | SHANGHAI KANGQIAO DENTAL INSTRUMENTS FACTORY |
| Owner/operator number | 9070000 |
| FEI number | 3004992978 |
| Address | 957 KANGQIAO ROAD, PUDONG |
| City | SHANGHAI |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DZC, DZN, EAX, ECN, ECS, EFK, EFL, EGN, EHP, EHY, EHZ, EID, EIF, EIG, EIK, EIR, EIS, EIX, EKB, EKC, EKE, EKH, EKI, EKJ, EKK, EKR, EKT, EMD, EMG, EMI and 24 more |
| Device classes | 1 |
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