Regulatory Disclaimer
No stem cell or cellular therapy is approved by the U.S. Food and Drug Administration (FDA) for the treatment of these conditions. The approaches described on this page are experimental, grounded in evolving translational and early clinical research, and offered only following comprehensive evaluation and informed consent.
References to "stem cells" on this page reflect cellular populations contained within autologous bone marrow–derived biologic material, not manufactured or expanded stem cell products.
Autologous bone marrow–derived cellular therapy is not approved by the U.S. Food and Drug Administration (FDA) as a drug or biologic for the treatment of specific musculoskeletal or systemic conditions. Clinical use is based on physician judgment, current scientific evidence, and individualized patient evaluation. No claims are made regarding guaranteed outcomes, tissue regeneration, or disease modification.
All biologic material is autologous (your own), patient-derived, and processed within the same procedural window. No expanded cell lines, donor cells, or research-only compounds.
Consistent with FDA guidance, we avoid unsupported claims regarding "stem cell" replacement or regeneration.
Platelet-rich plasma is an autologous biologic product prepared from a patient's own blood. PRP has not been approved by the U.S. Food and Drug Administration (FDA) for the treatment of specific diseases or musculoskeletal conditions. Clinical use is based on physician judgment, current scientific evidence, and individualized patient evaluation. No claims are made regarding guaranteed outcomes, tissue regeneration, or disease modification.