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FDA regulate latex and nitrile gloves (examination and surgical) as medical devices. Even though the gloves are class 1 device, it requires FDA 510K Clearance, Medical device establishment registration and device listing to market in the USA.Powdered gloves are not allowed to market in the USA for medical purpose.

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About Nitrile Medical Grade Gloves . Disposable gloves used during medical examinations in the medical field must have FDA approval. Meeting the safety requirements of the FDA means that the gloves are safe to use in the healthcare field. Their strength can withhold against and protect an individual against blood borne pathogens.

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Medical gloves are examples of personal protective equipment that are used to protect the wearer and/or the patient from the spread of infection or illness during medical procedures and examinations.

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Nitrile Gloves eliminate any potential for allergic to latex gloves because they are made of 100% nitrile. Nitrile Gloves offer three times the puncture resistance of latex gloves of comparable thickness and are resistant to a wider range of chemicals and provide greater resistance to blood borne pathogens as well.

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Footnotes and references: *GHX/ HPIS D_MAT2015 1 Caution: Gloves used for protection against chemotherapy drug and laboratory chemical exposure should be selected specifically for the type of chemicals being used. 2 This Cardinal Health product helps healthcare facilities comply with the USP <800> standard for the safe handling of hazardous drugs.. Note: Review Safety Data Sheets (SDS) …

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Mar 27, 2020·Does the FDA Require a 510K For Nitrile Gloves? Nitrile gloves, including for surgical use, are categorized as class 1 medical devices. This means they’re regulated by the FDA and require a 510(k) premarket notification. The FDA reviews the gloves to insure that they meet specific criteria related to safety and performance.

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