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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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308 records meeting your search criteria returned- Product Code: FZP Product Problem: Adverse Event Without Identified Device or Use Problem Report Date From: 01/1/2007
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ManufacturerBrand NameDate Report Received
DAVIS & GECK CARIBE LTD ENDO CLIP 03/05/2024
DAVIS & GECK CARIBE LTD ENDO CLIP 03/04/2024
DAVIS & GECK CARIBE LTD ENDO CLIP 03/04/2024
DAVIS & GECK CARIBE LTD ENDO CLIP III 02/12/2024
DAVIS & GECK CARIBE LTD ENDO CLIP III 02/12/2024
DAVIS & GECK CARIBE LTD ENDO CLIP II 11/16/2023
DAVIS & GECK CARIBE LTD ENDO CLIP 10/24/2023
ETHICON INC. LAPRA-TY SUTURE CLIP UNKNOWN PRODUCT 10/10/2023
DAVIS & GECK CARIBE LTD ENDO CLIP 10/05/2023
ETHICON ENDO-SURGERY, LLC. LIGAMAX-5MM ENDO CLIP APPLIER 10/03/2023
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