Establishment registration
SHENZHEN VIVOLIGHT MEDICAL DEVICE&TECHNOLOGY CO., LTD.
FDA establishment registration 3013351723 · shenzhen Guangdong, CN
Key facts
| Registration number | 3013351723 |
|---|---|
| Establishment name | SHENZHEN VIVOLIGHT MEDICAL DEVICE&TECHNOLOGY CO., LTD. |
| Owner/operator | Shenzhen Vivolight Medical Device&Technology Co., Ltd. |
| Owner/operator number | 10054042 |
| FEI number | 3013351723 |
| Address | Room 511-A, 5th Floor, Block B, Building R2, High-tech Industrial Park, No. 020, South Seventh Road |
| City | shenzhen Guangdong |
| Country | CN |
| Registration valid through | 2026 |
| Product codes listed | DQO, FSO, KZA, NQQ |
| Device classes | 1, 2 |
At a glance
- 1–9 Device listings
- 10–99 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