36 results · 24ms · Sources: EU EUDAMED, 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