Establishment registration
SHENZHEN BESTMAN INSTRUMENT CO.,LTD
FDA establishment registration 3008756262 · Shenzhen Guangdong, CN
Key facts
| Registration number | 3008756262 |
|---|---|
| Establishment name | SHENZHEN BESTMAN INSTRUMENT CO.,LTD |
| Owner/operator | Shenzhen Bestman Instrument CO.,Ltd |
| Owner/operator number | 10034759 |
| FEI number | 3008756262 |
| Address | 8th Floor, Yifang Building No.315 Shuangming Avenue, Guangming Street, Guangming District |
| City | Shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | KNG |
| Device classes | 2 |
At a glance
- 1–9 Device listings
- 1–9 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