Klaxon Mobility GmbH is one of 30 FDA 510(k) medical device manufacturers from Austria in the dataset, ranked by real submission volume.
Klaxon Mobility GmbH - FDA 510(k) Cleared Devices
Recent clearances: KLAXON (TWIST), Klaxon (Twist), KLICK (VARIANTS: POWER, RACE, MONSTER)
3
Total
3
Cleared
0
Denied
Klaxon Mobility GmbH has 3 FDA 510(k) cleared medical devices. Based in Arnoldstein, AT.
Latest FDA clearance: Apr 2025. Active since 2022. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Klaxon Mobility GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Klaxon-Mobility GmbH as regulatory consultant.
FDA 510(k) Regulatory Record - Klaxon Mobility GmbH
3 devices