Hartmann USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Hartmann USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Atrauman® Ag
1
Total
1
Cleared
0
Denied
Hartmann USA, Inc. has 1 FDA 510(k) cleared medical devices. Based in Rock Hill, US.
Latest FDA clearance: Dec 2024. Active since 2024. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Hartmann USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Qserve Group US as regulatory consultant.
FDA 510(k) Regulatory Record - Hartmann USA, Inc.
1 devices