Establishment registration
ORANTECH INC.
FDA establishment registration 3013783488 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3013783488 |
|---|---|
| Establishment name | ORANTECH INC. |
| Owner/operator | Orantech Inc. |
| Owner/operator number | 10058634 |
| FEI number | 3013783488 |
| Address | Zone#A,4F,1st Bld,7th Industrial Zone,Yulv Community, GongMing, Guangming New District, |
| City | Shenzhen Guangdong |
| Country | CN |
| Establishment types | Contract manufacturer |
| Registration valid through | 2026 |
| Product codes listed | BYH, BYX, CAE, CAI, CAT, CCK, CCL, DQA, DRG, DRQ, DRS, DRT, DRX, DSA, DSF, DSI, DSJ, DSK, DXG, DXN, DXQ, FLL, FQM, GDT, GEI, HFM, HFN, HGL, HGM, IKD and 10 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