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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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8 records meeting your search criteria returned- Product Code: KGO Patient Problem: Insufficient Information Report Date From: 01/1/2017
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ManufacturerBrand NameDate Report Received
MOLNLYCKE HEALTHCARE, US LLC BIOGEL INDICATOR UNDERGLOVE 12/29/2021
MOLNLYCKE HEALTHCARE, US LLC BIOGEL PL 11/19/2021
ALIMED, INC. FREEGUARD 08/27/2021
ANSELL HEALTHCARE PRODUCTS, LLC GAMMEX 06/21/2021
CARDINAL HEALTH 200, LLC PROTEXIS 04/26/2021
CARDINAL HEALTH 200, LLC PROTEXIS 10/29/2020
MEDLINE INDUSTRIES, INC. SENSICARE PI 10/16/2020
MEDLINE INDUSTRIES, INC. SENSICARE PI 10/16/2020
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