13 results
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28ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Morpheus RealTime Ultrasound, Pathway RealTime Ultrasound, QuickScan Bladder Ultrasound
FDA 510(k)
FDA Class 2
·Radiology
Oxford Partial Knee System
FDA UDI
Biomet Uk Ltd·05019279073030·Anatomic Meniscal Bearing
Right Medial
ILLUMIMED
FDA 510(k)
FDA Class 2
·Physical Medicine
GELPOINT PATH
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
RESTORATION ADM. INSERT
FDA Adverse Event
Injury
·STRYKER ORTHOPAEDICS CORK·Product code MEH·May 2, 2012
TMJ BILATERAL IMPLANTS
FDA Adverse Event
Injury
·TMJ SOLUTIONS, LLC DBA TMJ CONCEPTS·Product code LZD·August 25, 2022
OXF UNI TIB TRAY SZ AA RM PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·July 1, 2019
OXF TWIN-PEG CMNTD FEM XS PMA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·July 1, 2019
UNIFY QUADRA CRT-D
FDA Adverse Event
Injury
·ST. JUDE MEDICAL INC. CRMD·Product code NIK·January 13, 2014
CABLE CUTTER LRG
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXZ·June 11, 2013
M SERIES
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2011
OXFORD UNI TIB TRAY SZA RM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·June 17, 2025
OXFORD PH3 CEMENTLESS FEM SZ XSM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code NRA·June 17, 2025