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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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389 records meeting your search criteria returned- Product Code: GEI Product Problem: No Apparent Adverse Event Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
ARTHROCARE CORPORATION WEREWOLF FLOW 90 COBLATION WAND 01/11/2023
COVIDIEN MFG DC BOULDER FORCETRIAD 12/26/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/21/2022
ARTHROCARE CORPORATION ELIMINATOR ICW 12/20/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/13/2022
BAYLIS MEDICAL COMPANY INC. BAYLIS MEDICAL COMPANY RADIOFREQUENCY PU 12/13/2022
ETHICON ENDO-SURGERY, LLC. ENSEAL 45 CM SHAFT, CURVED JAW 11/22/2022
COVIDIEN MFG DC BOULDER VALLEYLAB FT10 11/18/2022
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