11 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FOUNDATION POROUS COATED HEMISPHERICAL SHELL
FDA 510(k)
FDA Class 2
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150690·K-WIRE - SINGLE TROCAR 0.9mm DIA x 75mm
SLS-88 TOTAL HIP SYSTEM, ACETABULAR CUP
FDA 510(k)
FDA Class 2
·Orthopedic
BUCCAL TUBE, BUCCAL ATTACHMENT
FDA 510(k)
FDA Class 1
·Dental
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FTL·June 16, 2006
BD CONNECTA¿ STOPCOCKS
FDA Adverse Event
Injury
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FMG·June 30, 2016
SECURE II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 22, 2013
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIVISION·Product code FNL·December 28, 2010
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·August 1, 2014
DIMENSION EXL 200
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC·Product code JJE·July 23, 2013
Hernia Pack, part number AMS3859
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017