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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K950204
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Product is labeled as LTX XP Miniplant, Dental Implant, Sterile. 2 09/18/2007 FEI # 1038806
Biomet 3i
LTX Endosseous Implant 6.0 mm X 11.5 mm and also LTX Endosseous Implant 5.0 mm X 15 mm, Sterile, 3 03/20/2003 FEI # 1038806
Implant Innovations, Inc.
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