Nikao

FDA Filings

This page includes the latest FDA filings for Nikao. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3005687068
FEI Number3005687068
NameNikao
Owner & OperatorNikao
Contact Address1880 North Commerce Pkwy.
Weston FL 33326 US
Official Correspondent
  • Edwin Aguilera
  • x-954-4244554-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1880 North Commerce Pkwy.
Weston, FL 33326 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Repack or Relabel Medical Device

FDA Filings

Device
Company
DeviceDate
Nikao
Venus Legacy2019-03-07
Nikao
Viva2017-02-20
Nikao
Legacy2016-04-07
Nikao
Neurova2015-03-18

Related Finance Registrations
DUNS833370641Nikao
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2018050851589Hong Kong,Hong Kong -> Los Angeles, CaliforniaLITHIUM BATTERY THIS SHIPMENT CONTAINS NO SO LID WOOD PACKING MATERIALS50 CTN
2018022054685Hong Kong,Hong Kong -> Los Angeles, CaliforniaLITHIUM BATTERY THIS SHIPMENT CONTAINS NO SO LID WOOD PACKING MATERIALS58 CTN
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