This page includes the latest FDA filings for Symatese Device. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.
| Registration Number | 3011224555 |
| FEI Number | 3011224555 |
| Name | Gordon MacFarlane |
| Owner & Operator | SYMATESE DEVICE |
| Contact Address | 135 Route Neuve IRIGNY FR-69 Rhone 69540 FR |
| US Agent |
|
| Registration Status | 1 |
| Initial Importer | N |
| Registration Expiration | 2020-04-25 |
| Registration Address | 2100 Pennbrook Pkwy North Wales, PA 19454 US |
| Establishment Type |
|
Device Company | Device | Date |
|---|---|---|
Gordon MacFarlane [SYMATESE DEVICE] | DOLPHIN Inflation Device | 2018-08-10 |
Gordon MacFarlane [SYMATESE DEVICE] | Traumacem V+ Syringe Kit | 2017-09-26 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - Mammotome | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - Hologic | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - BARD 7G | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | D750b Guiding Kit - BARD 10G | 2016-03-21 |
Gordon MacFarlane [SYMATESE DEVICE] | Vertecem V + Syringe kit | 2014-12-01 |
| NCAGE Code | FB7S3 | SYMATESE DEVICE |
| CAGE Code | FB7S3 | SYMATESE DEVICE |