Inomed GmbH is one of 142 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Inomed GmbH - FDA 510(k) Cleared Devices
Recent clearances: MICRO-RECORDING AND STIMULATION ELECTRODES-MICRO MACROELECTRODE MODEL NO. 230700-230799
1
Total
1
Cleared
0
Denied
Inomed GmbH has 1 FDA 510(k) cleared medical devices. Based in Se-103 93 Stockholm, SE.
Historical record: 1 cleared submissions from 2004 to 2004. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Inomed GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Inomed GmbH
1 devices