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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K142161
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Product Description
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FDA Recall
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ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2, Right Medial Catalog Number:M57220600... 2 10/21/2015 ConforMIS, Inc.
ConFormis iTotal CR Knee Replacement System- ITOTAL CR - IPOLY - IMPLANT KIT UNCAPTURED - LEFT ITO... 2 10/21/2015 ConforMIS, Inc.
ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR, Left Knee Catalog Numbe... 2 10/21/2015 ConforMIS, Inc.
ConFormis iTotal CR Knee Replacement System- iTOTAL CR, Right Knee Catalog Number: M57250600020 (U... 2 10/21/2015 ConforMIS, Inc.
ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL PS-IPOLY- IMPLANT KIT-LEFT a... 2 10/21/2015 ConforMIS, Inc.
Conformis iTotal Cruciate Retaining (CR) Knee Replacement System Model: TCR-111-1111 2 10/02/2018 ConforMIS, Inc.
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