Vivosens Biyoteknoloji Ar Ge San Tic L T D Sti

FDA Filings

This page includes the latest FDA filings for Vivosens Biyoteknoloji Ar Ge San Tic L T D Sti. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3015512211
FEI Number3015512211
NameDavid Lennarz
Owner & OperatorVivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti
Contact AddressResitpasa Mah. Katar Cad. Teknokent Ari 1 Sit. No: 2/5/15
Sariyer TR-34 Istanbul none TR
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address144 Research Drive
Hampton, VA 23666 US
Establishment TypeRemanufacture Medical Device



FDA Filings

Device
Company
DeviceDate
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03
David Lennarz [Vivosens Biyoteknoloji Ar-Ge, San. & Tic. Ltd. Sti]
Vivoo2019-10-03

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