ACTO GmbH is one of 470 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
ACTO GmbH - FDA 510(k) Cleared Devices
Recent clearances: Actolind® (06.3637. Actolind® Gel Plus)
1
Total
1
Cleared
0
Denied
ACTO GmbH has 1 FDA 510(k) cleared medical devices. Based in Braunschweig, DE.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by ACTO GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - ACTO GmbH
1 devices