Maxwell Sturgis

FDA Filings

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

FDA Registration(s)
Registration Number3003713161
FEI Number3003713161
NameMaxwell Sturgis
Owner & OperatorMITAKA KOHKI CO., LTD.
Contact AddressI-4, OHSAWA 5-CHOME --
MITAKA SHI, TOKYO JP-NOTA 181 JP
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address842 Oakridge Road N
Park City, UT 84098 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka OH62016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka OH52016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka OH42016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka MM51 YOH2016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka KestrelView2016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Mitaka KestrelView II2016-02-08
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
UniARM2012-10-12
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
UniARM2012-10-12
Maxwell Sturgis [MITAKA KOHKI CO., LTD.]
Point Setter2007-11-19

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