FDA 510(k) Applications Submitted by gel-e, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K180152 01/19/2018 gel-e Flex gel-e, Inc.
K192667 09/25/2019 gel-e Flex+ gel OTC gel-e, Inc.
K182811 10/03/2018 gel-e Flex+ gel-e, Inc.


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