Heager GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Heager GmbH has 1 FDA 510(k) cleared medical devices. Based in Haan, DE.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Heager GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Shanghai Truthful Information Technology Co., Ltd. as regulatory consultant.
1 devices