16 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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STRYKER NAVIGATION SYSTEM - NEURO MODULE, MODEL 6000-XXX-XXX
FDA 510(k)
FDA Class 2
·Neurology
artegral life
FDA UDI
Merz Dental GmbH·D7091993239·anteriors; shade B3; mould BOM
GOLDLENS(TM)
FDA 510(k)
FDA Class 2
·Ophthalmic
MPowRx Snoring Solution (also known as Good Morning Snore Solution)
FDA 510(k)
FDA Class 2
·Dental
ZEPHIR ANTERIOR CERVICAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC INC.·Product code KWQ·June 11, 2009
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·March 7, 2013
TOTALCARE BARIATRIC PLUS
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·January 21, 2011
ATTAIN OTW
FDA Adverse Event
Injury
·MPRI·Product code LWP·August 8, 2014
DURAL ALPHA INSERT W RIM II/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·March 12, 2019
DURASUL, ALPHA INSERT, HOODED, II/32
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LPH·September 28, 2018
METASUL, ALPHA INSERT, JJ/28
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·February 4, 2019
DURASUL, ALPHA INSERT, KK/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·March 13, 2018
WALLSTENT? RP ENDOPROSTHESIS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·July 21, 2025
COCR HEAD 32/ 0 'M' 12/14
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·June 4, 2019
DURASUL, ALPHA INSERT, LL/36
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code JDI·April 29, 2019
DURASUL, ALPHA INSERT, HOODED, KK/32
FDA Adverse Event
Malfunction
·ZIMMER GMBH·Product code LPH·June 15, 2018