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 Number: 3005111102
• FEI Number: 3005111102
• Name: CONTURA INTERNATIONAL A/S
• Owner & Operator: Contura International A/S
• Contact Address: Sydmarken 23 ; Soeborg DK-84 Region Hovedstaden 2860 DK
• Official Correspondent:
  • Carina Moldow
  • 45-811-00900-x
• US Agent:
  • Tim Kelp
  • Contura Inc
  • 949 9390539
  • tim.kelp@contura.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: Sydmarken 23 ; Soeborg Region Hovedstaden, 2860 DK
• Establishment Type: Manufacture Medical Device

FDA Filings

Device Company	Device	Date
PMA P170023S008 Contura International A/S	Bulkamid Urethral Bulking System	2021-01-14
PMA P170023S007 Contura International A/S	Bulkamid Urethral Bulking System	2020-12-17
PMA P170023S005 Contura International A/S	Bulkamid Urethral Bulking System	2020-12-02
PMA P170023S003 Contura International A/S	Bulkamid Urethral Bulking System	2020-10-22
PMA P170023S001 Contura International A/S	Bulkamid Urethral Bulking System	2020-06-02
GUDID 05704101500500 Contura International A/S	Bulkamid	2020-04-01
PMN P170023 | LNM CONTURA INTERNATIONAL A/S	Bulkamid Urethral Bulking System	2020-02-07
PMA P170023 Contura International A/S	Bulkamid Urethral Bulking System	2020-01-28