Contura I N T A S

FDA Filings

This page includes the latest FDA filings for Contura I N T 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 Number3005111102
FEI Number3005111102
NameCONTURA INTERNATIONAL A/S
Owner & OperatorContura International A/S
Contact AddressSydmarken 23
Soeborg DK-84 Region Hovedstaden 2860 DK
Official Correspondent
  • Carina Moldow
  • 45-811-00900-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressSydmarken 23
Soeborg Region Hovedstaden, 2860 DK
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Contura International A/S
Bulkamid Urethral Bulking System2020-06-02
Contura International A/S
Bulkamid 2020-04-01
CONTURA INTERNATIONAL A/S
Bulkamid Urethral Bulking System2020-02-07
Contura International A/S
Bulkamid Urethral Bulking System2020-01-28

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