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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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348 records meeting your search criteria returned- Product Code: GEH Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
BTG YOKNEAM ICESEED 90 DEGREE NEEDLE 03/27/2024
UNITED STATES ENDOSCOPY GROUP, INC. TRUFREEZE CONSOLE SYSTEM 03/22/2024
ICECURE MEDICAL LTD. PROSENSE CRYOABLATION SYSTEM 01/08/2024
BTG YOKNEAM ICEROD CX 90 DEGREE NEEDLE/VL 12/21/2023
ENTELLUS MEDICAL, INC. CLARIFIX 11/30/2023
ENTELLUS MEDICAL, INC. CLARIFIX 11/29/2023
ENTELLUS MEDICAL, INC. CLARIFIX 11/21/2023
ENTELLUS MEDICAL, INC. CLARIFIX 10/27/2023
BTG YOKNEAM ICEROD CX 90 DEGREE NEEDLE/VL 10/26/2023
BTG YOKNEAM ICESEED NEEDLE 10/05/2023
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