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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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32 records meeting your search criteria returned- Product Code: OAF Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
ENVOY MEDICAL CORP. ESTEEM 07/31/2023
ENVOY MEDICAL CORP. ESTEEM 05/10/2023
ENVOY MEDICAL CORPORATION ESTEEM 03/02/2023
ENVOY MEDICAL CORPORATION ESTEEM 12/21/2022
ENVOY MEDICAL CORPORATION ESTEEM 10/18/2022
ENVOY MEDICAL CORPORATION ESTEEM 10/11/2022
ENVOY MEDICAL CORPORATION ESTEEM 10/06/2022
ENVOY MEDICAL CORPORATION ESTEEM 09/14/2022
ENVOY MEDICAL CORPORATION ESTEEM 06/27/2022
ENVOY MEDICAL CORPORATION ESTEEM 05/16/2022
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