Semih Oktay

FDA Filings

This page includes the latest FDA filings for Semih Oktay. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3011632150
FEI Number3011632150
NameSemih Oktay
Owner & OperatorVeryan Medical
Contact AddressBlock 11, Galway Technology Park Parkmore
Galway IE-G Galway H91 VE0H IE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1783 Forest Drive, No. 254 Annapolis
Annapolis, MD 21401 US
Establishment TypeDevelop Specifications But Do Not Manufacture At This Facility



FDA Filings

Device
Company
DeviceDate
Semih Oktay [Veryan Medical]
BioMimics 3D Vascular Stent System2018-11-04

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