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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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5 records meeting your search criteria returned- Product Code: LWH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019
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ManufacturerBrand NameDate Report Received
STERIS ISRAEL SOLUTIONS LTD. OR LOCATE SPONGE SOLUTION 04/28/2023
COVIDIEN MFG DC BOULDER SITUATE 04/12/2022
DEPUY ORTHOPAEDICS INC US SROM*STM ST,36+8L NK,20X15X165 01/05/2021
MITG - RF SURGICAL SYSTEMS SITUATE 02/22/2019
MITG - RF SURGICAL SYSTEMS SITUATE 02/20/2019
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