48 results · 27ms · Sources: EU EUDAMED, US FDA

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Vivid S60N / Vivid S70N

FDA 510(k)
FDA Class 2 ·Radiology

Comprehensive® SRS

FDA UDI
Biomet Orthopedics, LLC·00880304522725·

PMT® Halo Systems

FDA UDI
PMT CORPORATION·00650551112273·HALO, 1203-5 VEST MEDIUM, LAMBSWOOL LINER, 1211...

Clavicle Plate

FDA UDI
I.T.S. GmbH·09120034304385·Clavicle Plate, 6-Hole

InSePtion MIS Fixation System

FDA UDI
Kalitec Direct LLC·B07314K0112160·Rasp, 16 and 18 mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523183821·2 Hole, 16 mm, Right, 1-Level Anterior Cervical...

OSSEOTITE 2 DENTAL IMPLANTS

FDA 510(k)
FDA Class 2 ·Dental

PVC FREE INTRAVASCULAR ADMINISTRATION SET

FDA 510(k)
FDA Class 2 ·General Hospital

COMPR SRS PROX BDY - SM 48MM

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWT·September 6, 2013

SYNCHROMED EL

FDA Adverse Event
Death ·RICE CREEK MANUFACTURING·Product code LKK·October 24, 2008

PYXIS ANESTHESIA SYSTEM (PAS)

FDA Adverse Event
Malfunction ·CAREFUSION·Product code BRY·July 12, 2011

RESOLUTION CLIP CLIPPING DEVICE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code MND·July 8, 2013

CONSTRAINED GLENOID 22MM LINER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·January 31, 2019

TM RVS BASE PLT 25MM POST +2

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code PHX·November 25, 2025

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019

MINI REVERSE GLENOID CONST

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HSD·April 30, 2019

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·June 19, 2019

NI

FDA Adverse Event
Injury ·BAXTER HEALTHCARE CORPORATION·Product code FTM·March 27, 2020