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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