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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K123705
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FDA Recall
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Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, ... 2 09/30/2021 FEI # 3002806725
Corin Ltd
Trinity Acetabular Shell Product Usage Total Hip Replacement. 2 04/22/2016 FEI # 1000131827
Corin USA Limited
Trinity Acetabular Shell Product Usage: Total Hip Replacement. 2 04/22/2016 FEI # 1000131827
Corin USA Limited
Trinity Acetabular System Product Usage - Total Hip Replacement. 2 04/22/2016 FEI # 1000131827
Corin USA Limited
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