Kinetic Instruments Inc

FDA Filings

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

FDA Registration(s)
Registration Number1294153
FEI Number1294153
NameKINETIC INSTRUMENTS, INC.
Owner & OperatorKINETIC INSTRUMENTS, INC.
Contact Address17 BERKSHIRE BLVD. --
Bethel CT 06801 US
Official Correspondent
  • WILLIAM J BECKER
  • x-203-7430080-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address17 BERKSHIRE BLVD.
BETHEL, CT 06801 US
Establishment Type
  • Manufacture Medical Device
  • Repack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
KINETIC INSTRUMENTS, INC.
VIPER2008-12-11
KINETIC INSTRUMENTS, INC.
VIPER2008-12-11
KINETIC INSTRUMENTS, INC.
PHOTON2001-11-09

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