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Medeon Biodesign, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K200902ClickCleanApril 30, 2020
K193652AbClose - Port Site Closure DeviceMarch 26, 2020
K192891Laparoscope Lens Shield Device (LENS)November 7, 2019
K170103Laparoscope Lens Shield Device (LENS)February 16, 2017
K160117AbClose - Port Site Closure DeviceSeptember 9, 2016
K160172Laparoscope Lens Shield DeviceApril 21, 2016
K151117Laparoscope Lens Shield DeviceAugust 20, 2015