24 results · 21ms · Sources: EU EUDAMED, US FDA

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TURBO PRIME IBD SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Altus Spine Pedicle Screw System

FDA UDI
Altus Spine, LLC·00843210132143·T25 Cannulated Locking Driver

Humelock II Cemented Shoulder System

FDA UDI
FX SOLUTIONS·03701037306413·HUMELOCK GUIDE Ø10mm

Novo Surgical

FDA UDI
NOVO SURGICAL, INC.·00842331101656·Titanium Rhoton Bipolar Forceps, round handles,...

Symmetry Rhoton®

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482139646·Rhoton Bipolar Forceps; Straight; Round Handle;...

Disposable Cuff

FDA UDI
SUNTECH MEDICAL, INC.·10840935105206·

Persona® PPS®

FDA UDI
Zimmer, Inc.·00889024631083·

Persona® PPS®

FDA UDI
Zimmer, Inc.·00889024631076·

BROTHERS POWDER-FREE VINYL EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

IMAGE IV DICOM IMAGE ARCHIVAL PACS NETWORK

FDA 510(k)
FDA Class 2 ·Radiology

FEMORAL ARRAY POST ASSEMBLY

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·February 18, 2020

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

INSYTE AUTOGUARD

FDA Adverse Event
Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·November 26, 2025

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 9, 2021

RIATA ACTIVE FIXATION

FDA Adverse Event
Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·April 26, 2013

POLYFLUX LR CAPILLARY DIALYZER

FDA Adverse Event
Malfunction ·GAMBRO DIALYSATOREN GMBH·Product code MSF·July 24, 2008