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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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66 records meeting your search criteria returned- Product Code: FTL Product Problem: Microbial Contamination of Device Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
W.L. GORE & ASSOCIATES GORE DUALMESH BIOMATERIAL 06/26/2018
W.L. GORE & ASSOCIATES GORE DUALMESH BIOMATERIAL 06/26/2018
W.L. GORE & ASSOCIATES GORE DUALMESH BIOMATERIAL 06/26/2018
ATRIUM MEDICAL C-QUR TACSHIELD 04/06/2018
ATRIUM MEDICAL C-QUR V-PATCH 04/06/2018
ATRIUM MEDICAL CORPORATION C-QUR V-PATCH 02/05/2018
ASPIDE MEDICAL SURGIMESH WN 01/19/2018
ATRIUM MEDICAL C-QUR V-PATCH 12/08/2017
ATRIUM MEDICAL C-QUR MESH 12/08/2017
SOFRADIM MESH FOR VENTRAL HERNIA 12/05/2017
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