Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Gel-E, Inc.

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories1
Latest FDA decision2019-10-25
TypeNumberDevice NameCodeDateActions
510(k) K192667 gel-e Flex+ gel OTCQSY2019-10-25 View
510(k) K182811 gel-e Flex+QSY2019-08-29 View
510(k) K180152 gel-e FlexQSY2018-06-22 View