Stryker Medtech K K

FDA Filings

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

FDA Registration(s)
Registration Number8043928
FEI Number3008319202
NameStryker Medtech K.K.
Owner & OperatorSTRYKER CORP.
Contact Address1901 Romence Pkwy
Portage MI 49002 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1131-1 HIGASHI NAGANUMA
INAGI Tokyo, 206-0802 JP
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Stryker Medtech K.K. [STRYKER CORP.]
WIRE CADDY2005-04-26
Stryker Medtech K.K. [STRYKER CORP.]
MANUAL SURGICAL INSTRUMENTS2005-04-26
Stryker Medtech K.K. [STRYKER CORP.]
LITe BIO Delivery System - Loading Tool2005-04-26
Stryker Medtech K.K. [STRYKER CORP.]
LITe BIO Delivery System - Loading Funnel2005-04-26
Stryker Medtech K.K. [STRYKER CORP.]
TPS2 Stand1992-12-15
Stryker Medtech K.K. [STRYKER CORP.]
THC5 Stand1992-12-15
Stryker Medtech K.K. [STRYKER CORP.]
Infusion Stand1992-12-15
Stryker Medtech K.K. [STRYKER CORP.]
IV Pole1992-12-15

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