Medeon Biodesign, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Medeon Biodesign, Inc. has 7 FDA 510(k) cleared medical devices. Based in Taipei, TW.
Historical record: 7 cleared submissions from 2015 to 2020. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Medeon Biodesign, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medeon Biodesign, Inc.
7 devices
Cleared
Apr 30, 2020
ClickClean
General & Plastic Surgery
27d
Cleared
Mar 26, 2020
AbClose - Port Site Closure Device
General & Plastic Surgery
87d
Cleared
Nov 07, 2019
Laparoscope Lens Shield Device (LENS)
General & Plastic Surgery
28d
Cleared
Feb 16, 2017
Laparoscope Lens Shield Device (LENS)
General & Plastic Surgery
35d
Cleared
Sep 09, 2016
AbClose - Port Site Closure Device
General & Plastic Surgery
234d
Cleared
Apr 21, 2016
Laparoscope Lens Shield Device
General & Plastic Surgery
85d
Cleared
Aug 20, 2015
Laparoscope Lens Shield Device
General & Plastic Surgery
115d