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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: K141065
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Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Vitrectomy Procedure... 2 07/10/2025 FEI # 1610287
Alcon Research LLC
Brand Name: Alcon Laboratories, Inc. Product Name: Constellation Vision System Combined Procedure P... 2 07/10/2025 FEI # 1610287
Alcon Research LLC
Constellation Vision System, REF: 8065751150 2 10/11/2023 FEI # 1000125771
Alcon Research, LLC
Constellation Procedure Pak 2 08/16/2023 FEI # 2523835
Alcon Research, LTD.
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