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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
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

 
 
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14 records meeting your search criteria returned- Product Code: KWI Product Problem: Patient-Device Incompatibility Report Date From: 01/1/2009
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ManufacturerBrand NameDate Report Received
ACUMED, LLC PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYME 09/22/2023
ACUMED, LLC PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYME 09/22/2023
ACUMED, LLC PROSTHESIS, ELBOW, HEMI-, RADIAL, POLYME 09/22/2023
ACUMED LLC 8.0MM X 0.0MM STEM 08/19/2020
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER 11/01/2018
WRIGHTS LANE SYNTHES USA PRODUCTS LLC PROSTHESIS, ELBOW, HEMI-RADIAL, POLYMER 11/01/2018
WRIGHT MEDICAL TECHNOLOGY, INC. EVOLVE(R) 10/03/2018
ACUMED LLC ARH SLIDE-LOC¿ STANDARD STEM 8MM 04/06/2018
ACUMED LLC ARH SLIDE-LOC HEAD 22MM, LEFT 04/06/2018
ACUMED LLC ARH SLIDE-LOC¿ NECK +1MM 04/06/2018
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