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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K201840
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AURORA Surgiscope System, Sterile, single use device that contains a Sheath, Obturator, and Imager. ... 2 03/06/2025 FEI # 3003418325
Integra LifeSciences Corp.
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