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Medline announces FDA clearance for REFLEX® HYBRID Nitinol Implants for foot and ankle surgery

  • Medline UNITE announced FDA 510 clearance for REFLEX HYBRID Nitinol Implant System on April 16, 2025.
  • This clearance allows Medline UNITE to expand its REFLEX portfolio for foot and ankle surgeries.
  • The REFLEX HYBRID combines a nitinol staple's compression with a locking plate's stability for fusions and procedures.
  • Scott Goldstein stated the product addresses gaps by offering specific designs, compression, and adjustment with nitinol.
  • Testing showed the HYBRID implant with a screw provided better load to failure results than traditional methods.
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Medline announces FDA clearance for REFLEX® HYBRID Nitinol Implants for foot and ankle surgery

Latest launch expands REFLEX® portfolio with additional options to deliver dynamic biplanar compression

·Valley City, United States
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Ortho Spine News | Your Trusted Voice for Medical Device Industry Ortho News broke the news in on Wednesday, April 16, 2025.
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