Shenzhen Vivolight Medical Device Technology Co L T D

FDA Filings

This page includes the latest FDA filings for Shenzhen Vivolight Medical Device Technology Co L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3013351723
FEI Number3013351723
NameAnny zhao
Owner & OperatorShenzhen Vivolight Medical Device&Technology Co; Ltd
Contact AddressRm. 201-2, Building 1, Liu Xiandong SCI&TECH Park, Nanshan District
shenzhen CN-44 Guangdong 518000 CN
Official Correspondent
  • Anna Wei
  • 86-755-86157558-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address4951 Netarts Hwy West
Tillamook, OR 97141 US
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Shenzhen Vivolight Medical Device & Technology Co., Ltd.
 VEINCAS 2023-04-28
Anny zhao [Shenzhen Vivolight Medical Device&Technology Co; Ltd]
VIVO 500S Projection Vein Finder2017-02-06
Anny zhao [Shenzhen Vivolight Medical Device&Technology Co; Ltd]
V800P Projection Vein Finder2017-02-06
Anny zhao [Shenzhen Vivolight Medical Device&Technology Co; Ltd]
V800F Projection Vein Finder2017-02-06

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