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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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119 records meeting your search criteria returned- Product Code: OCW Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2019

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ManufacturerBrand NameDate Report Received
APOLLO ENDOSURGERY COSTA RICA, SRL ENDOSCOPIC SUTURING SYSTEM 06/18/2021
APOLLO ENDOSURGERY COSTA RICA, SRL ENDOSCOPIC SUTURING SYSTEM 06/18/2021
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 05/07/2021
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 12/17/2020
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 12/10/2020
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 10/13/2020
APOLLO ENDOSURGERY OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 09/25/2020
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 06/16/2020
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 05/25/2020
APOLLO ENDOSURGERY, INC. OVERSTITCH ENDOSCOPIC SUTURING SYSTEM 04/13/2020
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