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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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106 records meeting your search criteria returned- Product Code: FTM Product Problem: Defective Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 07/14/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 06/09/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 06/02/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 06/01/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/30/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/11/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/09/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/07/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/04/2022
DAVOL INC., SUB. C.R. BARD, INC. XENMATRIX 05/03/2022
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