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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience
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12 records meeting your search criteria returned- Product Code: LQE Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
Unknown Manufacturer RAINDROP INLAY 01/12/2023
OPTICS MEDICAL / RVO 2.0, INC RAINDROP INLAY 03/16/2021
OPTICS MEDICAL / RVO 2.0, INC RAINDROP 02/26/2021
RVO 2.0, INC RAIN DROP NEAR VISION INLAY 12/19/2019
CORNEAGEN, INC. KAMRA CORNEAL INLAY 11/26/2019
Unknown Manufacturer KAMRA LENS 11/18/2019
REVISION / RVO 2.0, INC. RAINDROP UNDERLAY LENS 10/21/2019
REVISION OPTICS, INC. /RVO 2.0, INC. RAINDROP NEAR VISION INLAY 09/04/2019
RVO 2.0, INC. RAINDROP 08/07/2019
CORNEAGEN KAMRA INLAY 05/31/2019
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