Symatese Device

FDA Filings

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.

FDA Registration(s)
Registration Number3011224555
FEI Number3011224555
NameGordon MacFarlane
Owner & OperatorSYMATESE DEVICE
Contact Address135 Route Neuve
IRIGNY FR-69 Rhone 69540 FR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address2100 Pennbrook Pkwy
North Wales, PA 19454 US
Establishment Type
  • Manufacture Medical Device for Another Party (Contract Manufacturer)
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Gordon MacFarlane [SYMATESE DEVICE]
DOLPHIN Inflation Device2018-08-10
Gordon MacFarlane [SYMATESE DEVICE]
Traumacem V+ Syringe Kit2017-09-26
Gordon MacFarlane [SYMATESE DEVICE]
D750b Guiding Kit - Mammotome2016-03-21
Gordon MacFarlane [SYMATESE DEVICE]
D750b Guiding Kit - Hologic2016-03-21
Gordon MacFarlane [SYMATESE DEVICE]
D750b Guiding Kit - BARD 7G2016-03-21
Gordon MacFarlane [SYMATESE DEVICE]
D750b Guiding Kit - BARD 10G2016-03-21
Gordon MacFarlane [SYMATESE DEVICE]
Vertecem V + Syringe kit2014-12-01

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