Medical Device Manufacturer · US , St. Paul , MN

Lexion Medical, LLC - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2007

Recent clearances: AP50/30 Insufflator with Insuflow Port

13
Total
13
Cleared
0
Denied

Lexion Medical, LLC has 13 FDA 510(k) cleared obstetrics & gynecology devices. Based in St. Paul, US.

Historical record: 13 cleared submissions from 2007 to 2019.

Browse the complete list of FDA 510(k) cleared obstetrics & gynecology devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Hrg as regulatory consultant.

FDA 510(k) Regulatory Record - Lexion Medical, LLC

13 devices
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