66 results
·
17ms
·
Sources: EU EUDAMED, US FDA
ARTEC TWIST VALVE
FDA 510(k)
FDA Class 1
·Anesthesiology
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127020742·Full Hemisphere Reamer Size 56
Persona®
FDA UDI
Zimmer, Inc.·00889024559424·
PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
WORRY-REMOVER IRRIGATOR
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 31-34 POSTERIOR IOLS
M2A 38MM MOD HD -3MM NK
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·May 23, 2014
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·November 13, 2012
SIMPLEX P - US FULL DOSE 10-PK
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS LIMERICK·Product code LOD·September 7, 2010
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV31 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV40 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV40 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 31-34 POSTERIOR IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·POSTERIOR CHAMBER INTRAOCULAR LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·POSTERIOR CHAMBER INTRAOCULAR LENSES (TIER A SUBMISSION)
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLES 31-34 POSTERIOR IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV31 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV40 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·STYLE UV40 POSTERIOR CHAMBER LENS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·MODELS UV33A2 & UV33B2 J-LOOP INTRAOCULAR LENSES