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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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148 records meeting your search criteria returned- Product Code: OCW Patient Problem: Insufficient Information Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
DAVIS & GECK CARIBE LTD ENDO STITCH 05/09/2022
COVIDIEN COVIDIEN ENDO STITCH 05/03/2022
DAVIS & GECK CARIBE LTD ENDO STITCH 04/26/2022
DAVIS & GECK CARIBE LTD ENDO STITCH 04/26/2022
MEDTRONIC / COVIDIEN ENDO STITCH COVIDIEN 03/31/2022
DAVIS & GECK CARIBE LTD ENDO STITCH 03/31/2022
MEDTRONIC/ COVIDIEN ENDOSTITCH INSTRUMENT 03/15/2022
MEDTRONIC/ COVIDIEN ENDOSTITCH INSTRUMENT 03/15/2022
COVIDIEN LP ENDO STITCH 03/09/2022
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 03/02/2022
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