This page includes the latest FDA filings for Starfish Product Engineering Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3004186703 |
| FEI Number | 3004186703 |
| Name | Michael van der Woude |
| Owner & Operator | STARFISH PRODUCT ENGINEERING INC. |
| Contact Address | #455 Boleskine Road -- VICTORIA, B.C., CA-NOTA V8Z 1E7 CA |
| US Agent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2500 Bee Cave Road Building 1, Suite 300 Austin, TX 78746 US |
| Establishment Type | Manufacture Medical Device for Another Party (Contract Manufacturer) |
Device Company | Device | Date |
|---|---|---|
Michael van der Woude [STARFISH PRODUCT ENGINEERING INC.] | LEVO | 2014-11-04 |
Michael van der Woude [STARFISH PRODUCT ENGINEERING INC.] | SomnoMed MATRx | 2013-04-08 |
STARFISH PRODUCT ENGINEERING INC. | POD B-SCAN | 2007-04-11 |
| NCAGE Code | L0JT1 | STARFISH PRODUCT ENGINEERING INC |
| CAGE Code | L0JT1 | STARFISH PRODUCT ENGINEERING INC STARFISH MEDICAL |
| S.A.M. Registration | L0JT1 [241419188] | STARFISH PRODUCT ENGINEERING INC STARFISH MEDICAL |