Veryan Medical

FDA Filings

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

FDA Registration(s)

• Registration Number: 3011632150
• FEI Number: 3011632150
• Name: Semih Oktay
• Owner & Operator: Veryan Medical
• Contact Address: Block 11, Galway Technology Park Parkmore; Galway IE-G Galway H91 VE0H IE
• US Agent:
  • Semih Oktay
  • CardioMed Device Consultants LLC
  • 410 6742060
  • 410 6742133
  • soktay@cardiomedllc.com
• Registration Status: 1
• Initial Importer: N
• Registration Expiration: 2020-04-25
• Registration Address: 1783 Forest Drive, No. 254 Annapolis; Annapolis, MD 21401 US
• Establishment Type: Develop Specifications But Do Not Manufacture At This Facility

FDA Filings

Device Company	Device	Date
PMN P180003 | NIP Semih Oktay [Veryan Medical]	BioMimics 3D Vascular Stent System	2018-11-04

Similar & Related FDA Registered Companies

• VERYAN MEDICAL LIMITED
• Veryan Medical Ltd.unit 15, City Business Centre, Brighton Rdhorsham RH13 PMA NumberP180003 Supplement NumberS006 Date Received03/09/2022 Decision Date04/05/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Type30-day Notice Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No
• Veryan Medical Ltd.unit 15, City Business Centre, Brighton Rdhorsham RH13 PMA NumberP180003 Supplement NumberS005 Date Received10/14/2021 Decision Date03/01/2022 Product Code NIP  Advisory Committee Cardiovascular Supplement Typenormal 180 Day Track Supplement Reason Process Change - Manufacturer/sterilizer/packager/supplier Expedited Review Granted? No