Establishment registration
JINGFANG PRECISION MEDICAL DEVICE(SHENZHEN) CO., LTD.
FDA establishment registration 3014315088 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3014315088 |
|---|---|
| Establishment name | JINGFANG PRECISION MEDICAL DEVICE(SHENZHEN) CO., LTD. |
| Owner/operator | JingFang Precision Medical Device(Shenzhen) Co., Ltd. |
| Owner/operator number | 10056834 |
| FEI number | 3014315088 |
| Address | 301 Bldg C & 401 Bldg A, Jinweiyuan, No.41 Qingsong Rd, Zhukeng Community, Longtian Street, Pingshan District |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | OIJ |
| Device classes | 2 |
At a glance
- 1–9 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