Femasys Secures FDA Clearance for Next-Generation FemVue Controlled Device
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Femasys Inc. has received FDA 510(k) clearance for its FemVue Controlled device, a next-generation diagnostic tool for evaluating fallopian tube status. This device combines features from FemVue and FemChec technologies, enhancing clinical use and workflow efficiency. The news was originally published by Femasys via GlobeNewswire on December 18, 2025.
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