Kbd Inc

FDA Filings

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

FDA Registration(s)
Registration Number1022129
FEI Number1022129
NameKBD, INC.
Owner & OperatorKBD, INC.
Contact Address7240 W. Azure Drive, Ste. 160 --
Las Vegas NV 89130 US
Official Correspondent
  • Jessica Loggins
  • x-800-5443757-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address7240 W. Azure Drive Ste. 160
Las Vegas, NV 89130 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
KBD, INC.
Sperti Sunlamp Vitamin D Box2018-10-10

Related Finance Registrations
NCAGE Code0NPY7KBD INC
NCAGE Code48MG0KBD INC!DBA SPERTI SUNLAMP
CAGE Code0NPY7KBD INC
CAGE Code48MG0KBD INC SPERTI SUNLAMP
DUNS623909371KBD INC
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
2020070744689Shanghai ,China (Mainland) -> Long Beach, CaliforniaFLUORESCENT SELF-TANNING74 CTN
2018111020643Vung Tau,Vietnam -> New York/Newark Area, Newark, New Jersey1 PKG = 1 PLT NAME OF COMMODITY SPECIFICATION : CEMENT TILES HS CODE: 6810 11001 PKG

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