Simex Medizintechnik GmbH is one of 489 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Simex Medizintechnik GmbH - FDA 510(k) Cleared Devices
Recent clearances: FloSure Ventilation Patch, SIMEX SUBGLOTTIC ASPIRATION SYSTEM, SIMEX NEGATIVE PRESSURE WOUND THERAPY POWERED SUCTION PUMPS SERIES: SIM-EX200 AND SIM-EX300
3
Total
3
Cleared
0
Denied
Simex Medizintechnik GmbH has 3 FDA 510(k) cleared medical devices. Based in Deisslingen, DE.
Historical record: 3 cleared submissions from 2012 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Simex Medizintechnik GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Flosure Technologies, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Simex Medizintechnik GmbH
3 devices