Establishment registration
EDAN INSTRUMENTS, INC.
FDA establishment registration 3003971136 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3003971136 |
|---|---|
| Establishment name | EDAN INSTRUMENTS, INC. |
| Owner/operator | EDAN INSTRUMENTS, INC. |
| Owner/operator number | 9055347 |
| FEI number | 3003971136 |
| Address | #15 Jinhui Road, Jinsha Community |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | BZK, BZQ, CBQ, CBR, CBS, CCK, CCL, CEM, CGZ, CHL, DPS, DPW, DQA, DQK, DRG, DRT, DSA, DSB, DSF, DSH, DSI, DSJ, DSK, DXN, DYC, FLL, GKF, GLK, GXY, GZJ and 26 more |
| Device classes | 1, 2 |
At a glance
- 10–99 Device listings
- 1,000+ 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