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FDA 510(k) Applications Submitted by Medeon Biodesign, Inc
FDA 510(k) Number
Submission Date
Device Name
Applicant
K170103
01/12/2017
Laparoscope Lens Shield Device (LENS)
Medeon Biodesign, Inc
K160117
01/19/2016
AbClose - Port Site Closure Device
Medeon Biodesign, Inc
K160172
01/27/2016
Laparoscope Lens Shield Device
Medeon Biodesign, Inc
K151117
04/27/2015
Laparoscope Lens Shield Device
Medeon Biodesign, Inc
K192891
10/10/2019
Laparoscope Lens Shield Device (LENS)
Medeon Biodesign, Inc
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