Sixarp L L C Praxis

FDA Filings

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

FDA Registration(s)
Registration Number1000115322
FEI Number1000115322
NameSixarp LLC, Praxis
Owner & OperatorSixarp LLC, Praxis
Contact Address7650 Caterpillar Dr Suite D
Grand Rapids MI 49548 US
Official Correspondent
  • Richard A King
  • x-616-8278525-x
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address7650 Caterpillar Ct SW Ste D
Grand Rapids, MI 49548 US
Establishment TypeRepack or Relabel Medical Device



FDA Filings

Device
Company
DeviceDate
Sixarp LLC, Praxis
AgaMatrix2011-12-09
Sixarp LLC, Praxis
AgaMatrix2011-12-09
Sixarp LLC, Praxis
AgaMatrix2011-12-09

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