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BioStem Technologies, Inc. products are registered under the regulations of the U.S. Food and Drug Administration (FDA) governing the manufacture and distribution of Human Tissue Products. They are marketed as structural tissue allografts for homologous use and are used by physicians as barriers, wound coverings, conduits, and/or cushions in the treatment of their patients.
  • Our Technologies
    • CryoTek®
    • SteriTek®
    • BioRetain®
    • Procurement
  • Our Products
    • Advanced Surgical Care
      • Clarix® 1K
    • Advanced Wound Care
      • Neox® 1K
      • Neox® RT
      • Vendaje AC®
      • American Amnion ACTM
  • Clinical Evidence
  • Company
    • About Us
    • Leadership
    • Facilities & Quality
    • News & Events
    • Careers
  • Resources
    • AATB Accreditation
    • FDA Registration
    • State Registrations
    • Application Guides
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  • PHYSICIAN PORTAL
  • CONTACT US
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