Arrinex Inc

FDA Filings

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

FDA Registration(s)
Registration Number3015132143
FEI Number3015132143
NameArrinex, INC
Owner & OperatorSTRYKER CORP.
Contact Address1901 Romence Pkwy
Portage MI 49002 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address127 Independence Drive
Menlo Park, CA 94025 US
Establishment TypeManufacture Medical Device



Registration Number3015144674
FEI Number3015144674
NameArrinex, Inc
Owner & OperatorSTRYKER CORP.
Contact Address1901 Romence Pkwy
Portage MI 49002 US
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address3503-3505 Haven Avenue
Menlo Park, CA 94025 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
ARRINEX, INC.
ClariFix CFX-10022019-12-10
ARRINEX, INC.
ClariFix CFX-10002019-12-10
ARRINEX, INC.
ClariFix 2019-12-03
Arrinex, Inc [STRYKER CORP.]
ClariFix2019-11-22
Arrinex, INC [STRYKER CORP.]
ClariFix2019-11-22
Arrinex, Inc [STRYKER CORP.]
ClariFix Device2019-03-26
Arrinex, INC [STRYKER CORP.]
ClariFix Device2019-03-26
Arrinex, Inc
ClariFix2019-02-26
ARRINEX, INC.
ClariFix 2018-05-07
ARRINEX, INC.
ClariFix 2018-05-07
ARRINEX, INC.
ClariFix Device2017-02-14
ARRINEX, INC.
ClariFix Device2016-06-24

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