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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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101 records meeting your search criteria returned- Product Code: OCW Patient Problem: Foreign Body In Patient Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
COVIDIEN LP ENDO STITCH 09/02/2021
DAVIS & GECK CARIBE LTD ENDO STITCH 07/19/2021
COVIDIEN LP LLC NORTH HAVEN ENDO STITCH 07/16/2021
DAVIS & GECK CARIBE LTD SURGIDAC 07/14/2021
MEDTRONIC/COVIDIEN MEDTRONIC/COVIDIEN ENDOSTITCH DEVICE 07/01/2021
COVIDIEN POLYSORB O ES-9 SUTURE 04/27/2021
COVIDIEN ENDOSTITCH AUTO SUTURE 11/02/2020
DAVIS & GECK CARIBE LTD SURGIDAC 10/27/2020
DAVIS & GECK CARIBE LTD POLYSORB 10/05/2020
DAVIS & GECK CARIBE LTD POLYSORB 10/02/2020
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