18 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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RIGI-FIX HIP STEM SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00721011·
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776299637·McGowan Style Suction Hemorroid Ligator
ConMed Linvatec
FDA UDI
Provision·B504OM50721010·
N/A
FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·00885825012069·Sagittal Saw Blade
STRYKER 2000
FDA UDI
Conmed Corporation·10845854004067·LARGE BONE, HALL BLADE, OSCILLATING, ME-92 COAT...
NA
FDA UDI
STERILMED, INC.·10888551020992·SAW BLADE SAGITTAL LARGE BONE
SPACELABS HEALTHCARE
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522102493·MICRO-V ALTERNANS SENSOR(MV4),POUCH OF 7,UDI
Spacelabs Healthcare
FDA UDI
SPACELABS HEALTHCARE (WASHINGTON), INC·10841522121753·MICRO-V ALTERNANS SENSOR(MV4),POUCH OF 7,UDI
MEDTEXX POWDERFREE NITRILE RUBBER EXAMINATION GLOVES, GREEN COLOUR
FDA 510(k)
FDA Class 1
·General Hospital
ANGIODYNAMICS ABSCESSION BILIARY DRAINAGE CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CANNULATED PARTIALLY THREADED RECONSTRUCTIVE SCREW
FDA Adverse Event
Injury
·BIOMET·Product code HSB·March 13, 2012
GII OVAL RESURFACING PAT 32MM
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code JWH·December 18, 2015
SM204 M-SERIES W/BIG WHEEL
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·April 21, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013
SPRINT
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 2008
NONIN
FDA Adverse Event
Other
·CAREFUSION 211, INC.·Product code DQA·December 13, 2010
Philips Zenition 70, Model Number: 718133
FDA Enforcement
Class II
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·November 20, 2024