Spectrum Assembly Inc

FDA Filings

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

FDA Registration(s)
Registration Number3002672225
FEI Number3002672225
NameSPECTRUM ASSEMBLY INC.
Owner & OperatorSPECTRUM ASSEMBLY INC.
Contact Address6300 Yarrow Dr Suite 100
Carlsbad CA 92011 US
Official Correspondent
  • MICHAEL - BALDWIN
  • x-760-9304000-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address6300 Yarrow Dr SUITE 100
Carlsbad, CA 92011 US
Establishment TypeManufacture Medical Device for Another Party (Contract Manufacturer)

FDA Filings

Device
Company
DeviceDate
SPECTRUM ASSEMBLY INC.
Med4 Elite2019-11-04
SPECTRUM ASSEMBLY INC.
Med4 Elite2019-11-04
SPECTRUM ASSEMBLY INC.
Del Sol Red Light Therapy System2019-11-04
SPECTRUM ASSEMBLY INC.
Del Sol Blue Light Therapy System2019-11-04
SPECTRUM ASSEMBLY INC.
Skylit Phototherapy System2017-10-11

Related Finance Registrations
NCAGE Code6GFJ8SPECTRUM ASSEMBLY INC
CAGE Code6GFJ8SPECTRUM ASSEMBLY INC
U.S. Import Records [external site]
Import IDShipmentCargo DescriptionQuantity
201906048938Southhampton,United Kingdom -> Los Angeles, CaliforniaXRAY MACHINE1 CRT
2019031331469Anvers,Belgium -> Long Beach, CaliforniaMEDICAL CARHOPS20 PKG
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