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.
Registration Number | 3003713161 |
FEI Number | 3003713161 |
Name | Maxwell Sturgis |
Owner & Operator | MITAKA KOHKI CO., LTD. |
Contact Address | I-4, OHSAWA 5-CHOME -- MITAKA SHI, TOKYO JP-NOTA 181 JP |
US Agent |
|
Registration Status | 1 |
Initial Importer | N |
Registration Expiration | 2020-04-25 |
Registration Address | 842 Oakridge Road N Park City, UT 84098 US |
Establishment Type | Manufacture Medical Device |
Device Company | Device | Date |
---|---|---|
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka OH6 | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka OH5 | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka OH4 | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka MM51 YOH | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka KestrelView | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Mitaka KestrelView II | 2016-02-08 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | UniARM | 2012-10-12 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | UniARM | 2012-10-12 |
Maxwell Sturgis [MITAKA KOHKI CO., LTD.] | Point Setter | 2007-11-19 |