Kaneka Pharma America LLC

FDA Filings

This page includes the latest FDA filings for Kaneka Pharma America LLC. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Kaneka Pharma America LLC holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number2435151
FEI Number2435151
NameKANEKA PHARMA AMERICA LLC
Owner & OperatorKANEKA CORP.
Contact Address2-3-18, Nakanoshima, Kita-ku
Osaka JP-27 Osaka 530-8288 JP
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address546 FIFTH AVE., 21ST FLOOR
New York, NY 10036 US



FDA Filings

Device
Company
DeviceDate
Kaneka Pharma America LLC
I-ED COIL2020-04-25
KANEKA PHARMA AMERICA LLC
TUBING SYSTEM FOR PLASMAPHERESIS 2018-09-21
KANEKA PHARMA AMERICA LLC
SULFLUX 2018-05-30
KANEKA PHARMA AMERICA LLC
TUBING SYSTEM FOR PLASMAPHERESIS 2018-05-29
KANEKA PHARMA AMERICA LLC
APHERESIS MACHINE 2018-05-29
KANEKA PHARMA AMERICA LLC
Lacriflow CL2017-04-18
KANEKA PHARMA AMERICA LLC
XPRESSWAY RX CATHETER (6F LD-VERISON)2012-07-30
KANEKA PHARMA AMERICA LLC
KANEKA PHARMA AMERICA XPRESS-WAY RX2010-10-22

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