66 results · 17ms · Sources: EU EUDAMED, US FDA

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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