33 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

EUB-5500 DIAGNOSTIC ULTRASOUND SCANNER

FDA 510(k)
FDA Class 2 ·Radiology

Baltic Denture System BD Load

FDA UDI
Merz Dental GmbH·D7091032503·Baltic Denture System BDLoad ↓ Mw7 PLSEum2DFm C...

ebner 502 Handle 30 degree Up Head Angle

FDA UDI
MAXILON LABORATORIES INC·00860002195049·The ebner 502 expanded bone grafter is intended...

ACE Surgical Chgut3-0 30"/75c Ds24

FDA UDI
Surgical Specialties México, S. de R.L. de C.V.·00848782022960·003-2503 Chgut3-0 30"/75c Ds24

CosmoLock Pedicle Screw System

FDA UDI
Kalitec Direct LLC·B07311K0315030·Probe, 1.5 inch Ball, Steffee, Curved, Impaction

METAL SCREW ANCHOR

FDA 510(k)
FDA Class 2 ·Orthopedic

FETALGARD LITE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

AMINGO

FDA Adverse Event
Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 9, 2016

SMART MONITOR 2 PS

FDA Adverse Event
Malfunction ·PHILIPS RESPIRONICS -CHMV·Product code NPF·August 26, 2014

AMINGO

FDA Adverse Event
Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 30, 2016

AMINGO

FDA Adverse Event
Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·December 29, 2016

AMINGO

FDA Adverse Event
Malfunction ·DATEX-OHMEDA, INC.·Product code BSZ·January 4, 2017

CHARGING SYSTEM

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 1, 2013

UNKNOWN PUMP

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·March 24, 2011

4.0MM 90-S MAX SERFAS ENERGY SUCTION PROBE

FDA Adverse Event
STRYKER ENDOSCOPY PUERTO RICO·Product code GEI·April 16, 2008

UNKNOWN HIP

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWA·February 3, 2016

SMART MONITOR 2 PS

FDA Adverse Event
Malfunction ·PHILIPS RESPIRONICS - CHMV·Product code NPF·May 30, 2013

E-POLY 40MM MAXROM LNR SZ26

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·April 24, 2014

SELEX/MAGNUM MOD HD 40MM +9

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LZO·April 24, 2014

E-POLY 40MM MAXROM LNR SZ28

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·April 24, 2014