The Dr. PRP Process
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Regulatory Information
Dr. PRP USA’s PRP kits are FDA 510(k) cleared medical devices for the preparation of autologous platelet-rich plasma (PRP) at the point of care. This clearance reflects the FDA’s determination that the devices are substantially equivalent to legally marketed predicate devices for their cleared indications.
Dr. PRP USA is committed to providing healthcare professionals with high-quality PRP preparation systems that meet applicable regulatory requirements and support consistent clinical workflows.
