KALR STORZ SE & Co. KG is one of 467 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
KALR STORZ SE & Co. KG - FDA 510(k) Cleared Devices
Recent clearances: KARL STORZ TIPCAM1 Rubina
1
Total
1
Cleared
0
Denied
KALR STORZ SE & Co. KG has 1 FDA 510(k) cleared medical devices. Based in Tuttlingen, DE.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by KALR STORZ SE & Co. KG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - KALR STORZ SE & Co. KG
1 devices