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U.S. Department of Health and Human Services

Manufacturer and User Facility Device Experience (MAUDE)
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23 records meeting your search criteria returned- Product Code: MBI Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2007

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ManufacturerBrand NameDate Report Received
ARTHREX, INC. H/W INTERNALBRACE LGMNT AUGMNT REPR KIT 07/28/2020
MEDOS INTERNATIONAL SARL TRUESPAN 24 DEGREE PEEK 07/13/2020
ARTHREX, INC. FIBERTAK 10/11/2019
ARTHREX, INC. PROXIMAL TENODESIS IMPLANT SYSTEM REV: 0 06/26/2019
SMITH & NEPHEW, INC. TWINFIX ULTRA 5.5MM W/2 UB (WHT & BLUE) 04/12/2019
ARTHREX, INC. FIBERTAK DOUBLE LOADED W/ 1.3 SUTURETAPE 07/13/2018
STRYKER ENDOSCOPY-SAN JOSE ICONIX 1 NEEDLES WITH INTELLIBRAID TECHN 03/13/2018
STRYKER PEEK IMPLANT 09/13/2017
BIOMET SPORTS MEDICINE UNKNOWN JUGGERKNOT 11/10/2016
BIOMET SPORTS MEDICINE JUGGERKNOT 1.4 SHORT W/ NDLS 11/10/2016
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