Vitromed Langenfeld is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Vitromed Langenfeld - FDA 510(k) Cleared Devices
Recent clearances: V-HEPES PLUS
1
Total
1
Cleared
0
Denied
Vitromed Langenfeld has 1 FDA 510(k) cleared medical devices. Based in Langenfeld, DE.
Last cleared in 2022. Active since 2022. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Vitromed Langenfeld Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Specialists, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Vitromed Langenfeld
1 devices