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Zdrowie i gospodarka · 01/06/2026

FDA Classifies Orally Ingested Transient Device for Constipation into Class II

The FDA has classified the orally ingested transient device for constipation into Class II, a category that requires special controls to ensure safety and effectiveness, aiming to enhance patient access to innovative devices while reducing regulatory burdens.

Source: Federal Register — Health and Human ServicesOpen original release →