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Xiros Limited

FDA 510(k) & PMA Approved Devices — 1 products

Total Devices1
Categories1
Latest FDA decision2025-07-15
TypeNumberDevice NameCodeDateActions
510(k) K242237 Jewel Soft Tissue Reinforcement Device (102-6005)QUW2025-07-15 View

Related Clinical Trials

NCT05264389Post-market Clinical Follow-up (PMCF) Study of the Poly-Tape Devices for Medial Patellofemoral Ligament (MPFL) ReconstructionACTIVE_NOT_RECRUITINGNCT05906004Post-Market Clinical Follow-up (PMCF) Study of the Pitch-Patch for the Augmentation or Reinforcement of the Rotator CuffRECRUITINGNCT05304819PMCF Study of the AchilloCordPLUS System Implant Set for Acute Achilles Tendon RepairCOMPLETED
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