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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K160405
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BeamAdjust software Version 2.3.3 Ref: S080032 The following devices are affected when a relative... 2 09/11/2023 FEI # 3007360740
PTW-FREIBURG
Software BeamAdjust version 2.2, Catalog No: S070009 Software VeriSoft version 8.0, Catalog No: S08... 2 01/11/2022 FEI # 3019665367
PTW NORTH AMERICA CORPORATION
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