Vitromed GmbH - FDA 510(k) Cleared Devices

Vitromed GmbH has 7 FDA 510(k) cleared medical devices. Based in Jena, DE.

Latest FDA clearance: Mar 2025. Active since 2020. Primary specialty: Obstetrics & Gynecology.

Browse the FDA 510(k) cleared devices submitted by Vitromed GmbH Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Regulatory Specialists, Inc. as regulatory consultant.