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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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16 records meeting your search criteria returned- Product Code: OCW Product Problem: Defective Device Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
COVIDIEN LP ENDO STITCH 07/12/2019
COVIDIEN LP ENDO STITCH 07/10/2019
COVIDIEN LP ENDO STITCH 02/07/2019
COVIDIEN LP ENDO STITCH 02/07/2019
COVIDIEN LP ENDO STITCH 02/01/2019
COVIDIEN ENDO STITCH* 10MM SUTURING DEVICE 07/14/2015
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