Response Ortho Teknolojik Uretim A S

FDA Filings

This page includes the latest FDA filings for Response Ortho Teknolojik Uretim A S. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014702378
FEI Number3014702378
NameResponse Ortho Teknolojik Uretim A.S.
Owner & OperatorWishBone Medical Inc.
Contact Address2150 North Pointe Dr.
Warsaw IN 46582 US
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressITOSB, 10. Cadde, NO:1
Tuzla Istanbul, 34959 TR
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Response Ortho Teknolojik Uretim A.S. [WishBone Medical Inc.]
WishBone Medical Plates and Screws System2018-11-27
Response Ortho Teknolojik Uretim A.S. [WishBone Medical Inc.]
WishBone Medical Plates and Screws System2018-11-27

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