Atmos Medizintechnik GmbH & Co. KG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Atmos Medizintechnik GmbH & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: ATMOS C 051 Thorax (317.0200.0), ATMOS Scope (507.7000.0)
2
Total
2
Cleared
0
Denied
Atmos Medizintechnik GmbH & Co. KG has 2 FDA 510(k) cleared medical devices. Based in Lenzkirch, DE.
Latest FDA clearance: Mar 2025. Active since 2023. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Atmos Medizintechnik GmbH & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Atmos Medizintechnik GmbH & Co. KG
2 devices