36 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Panthera Dental Milled Bars
FDA 510(k)
FDA Class 2
·Dental
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463240·
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260544·
Sonic
FDA UDI
Sonic Innovations, Inc.·05711583032580·ET40, KIT 312 NFM 90 PB R BE ENCHANT 40
Aspida
FDA UDI
ALPHATEC SPINE, INC.·00840967190914·LUMBAR DTS GUIDE 8MM
Orthos
FDA UDI
ORMCO CORPORATION·00889989030204·ORTHOS CM TMA ARCH 016X022 LOSM PK10
CLICKFINE PEN NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
TRUSS THORACOLUMBAR PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
FASTTAKE
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·May 13, 2003
CYTOMAX II DOUBLE LUMEN CYTOLOGY BRUSH
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code FDX·February 22, 2021
SHELL POROUS WITHOUT HOLES 54 MM O.D.
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·April 11, 2019
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·October 7, 2008
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·August 4, 2011
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 20, 2013
LINER STANDARD 3.5 MM OFFSET 36 MM I.D. FOR USE WITH 50/52/54 MM O.D. SHELLS
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·January 3, 2019
FUSION CYTOLOGY BRUSH
FDA Adverse Event
Malfunction
·COOK ENDOSCOPY·Product code FDX·January 6, 2022
FUSION CYTOLOGY BRUSH
FDA Adverse Event
Injury
·COOK ENDOSCOPY·Product code FDX·October 25, 2021
CYTOMAX II DOUBLE LUMEN CYTOLOGY BRUSH
FDA Adverse Event
Injury
·WILSON-COOK MEDICAL INC·Product code FDX·May 4, 2022
CYTOMAX II DOUBLE LUMEN CYTOLOGY BRUSH
FDA Adverse Event
Injury
·WILSON-COOK MEDICAL INC·Product code FDX·November 14, 2022
G7 VIT E NEUTRAL LNR 36MM E
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·May 6, 2022