Notice 6 Jun 2025 compliance, healthcare, fda, medical devices, labeling, hernia mesh

📦FDA Draft Guidance on Hernia Mesh Package Labeling Recommendations

The Food and Drug Administration (FDA or Agency) is announcing the availability of the draft guidance entitled "Hernia Mesh--Package Labeling Recommendations." This draft guidance provides labeling recommendations for hernia mesh devices that are intended to help promote the safe and effective use of hernia mesh. This draft guidance is not final nor is it for implementation at this time.

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