Litex Manufacturing Inc

FDA Filings

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

FDA Registration(s)
Registration Number3010676465
FEI Number3010676465
NameLitex Manufacturing, Inc.
Owner & OperatorLitex Manufacturing, Inc.
Contact Address1501 Sunshine Drive
Glendale CA 91208 US
Official Correspondent
  • Noel Gharibian
  • x-818-6427822-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address820 Thompson Ave Ste 9
Glendale, CA 91201 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Litex Manufacturing, Inc.
Operating Room Universal Light Handle2014-10-08
Litex Manufacturing, Inc.
Operating Room Universal Light Camera Adator2014-10-08
Litex Manufacturing, Inc.
Operating Room Universal Light Adaptor2014-10-08
Litex Manufacturing, Inc.
Operating Room Light Handle Adapter2014-09-29
Litex Manufacturing, Inc.
Devon2014-01-10

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