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U.S. Department of Health and Human Services

MAUDE - Manufacturer and User Facility Device Experience

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510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
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179 records meeting your search criteria returned- Product Code: MBI Patient Problem: Unspecified Tissue Injury Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
MEDOS INTERNATIONAL SàRL RGDLOOP ADJUSTABLE LONG 08/31/2023
MEDOS INTERNATIONAL SàRL 4.9MM HEALX ADV SP PEEK ANCHOR 08/31/2023
ZIMMER BIOMET, INC. JUGGERSTITCH CURVED IMPLANT 08/28/2023
SMITH & NEPHEW, INC. UNKNOWN SMITH+NEPHEW DEV 08/28/2023
SMITH & NEPHEW, INC. UNKN ULTRABUTTON DEV 08/26/2023
ARTHROCARE CORPORATION UNKNOWN ULTRABUTTON DEV 08/25/2023
ARTHROCARE CORPORATION UNKNOWN ULTRABUTTON DEVICE 08/11/2023
SMITH & NEPHEW, INC. UNKN JOINT REPAIR DEV 07/17/2023
SMITH & NEPHEW, INC. UNKNOWN JOINT REPAIR DEVICE 07/14/2023
MEDOS INTERNATIONAL SàRL TRUESPAN 12 DEGREE PEEK 07/13/2023
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