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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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82 records meeting your search criteria returned- Product Code: FTL Product Problem: Use of Device Problem Report Date From: 01/1/2016
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ManufacturerBrand NameDate Report Received
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ECHO 03/07/2017
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ECHO 02/28/2017
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ECHO 11/23/2016
BARD SHANNON LIMITED -3005636544 VENTRALIGHT ST W/ECHO 11/03/2016
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ECHO 09/30/2016
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ECHO 08/10/2016
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ ECHO 06/01/2016
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST W/ ECHO 02/29/2016
TYRX, INC. AIGIS-R LARGE 02/09/2016
DAVOL INC., SUB. C.R. BARD, INC. VENTRALIGHT ST MESH 01/25/2016
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