Endoplus is one of 22572 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Endoplus - FDA 510(k) Cleared Devices
Recent clearances: ENDOPLUS hand-held laparoscopic instruments
1
Total
1
Cleared
0
Denied
Endoplus has 1 FDA 510(k) cleared medical devices. Based in Mundelein, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Endoplus Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smith Assoicates as regulatory consultant.
FDA 510(k) Regulatory Record - Endoplus
1 devices