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 |