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Corin Ltd

5 FDA 510(k) clearances · Recalling firm

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RecordFirmDate
Unity CR Femur Right, Size 6, Model Number 112.001.32 Primary and revision total knee arth recall (Z-0213-2024)Corin Ltd2023-11-02
Unity Total Knee System, Model Number 112.001.34. Primary and revision total knee arthropl recall (Z-0214-2024)Corin Ltd2023-11-02
Corin BIOLOX DELTA MOD HEAD,032mm, EX LONG +7mm, REF 104.3215 recall (Z-0726-2023)Corin Ltd2022-12-19
Corin BIOLOX DELTA MOD HEAD, 036mm EX LONG +8mm, REF 104.3615 recall (Z-0727-2023)Corin Ltd2022-12-19
Unity Total Knee System. Used for knee prosthesis in total knee replacement recall (Z-0273-2023)Corin Ltd2022-11-21

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Every clearance here is in the API, with alerts when new ones post.