32 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.

TENS & PMS

FDA 510(k)
FDA Class 2 ·Physical Medicine

AGXO

FDA UDI
Oticon A/S·05707131356314·G500 S, MINIRITE R LI-ION 2.4G C063 AGXO

Dornier MedTech

FDA UDI
DORNIER MEDTECH AMERICA, INC.·04049958003196·1000 micron Holmium Laser Fiber Cable, Reusable...

24PW - Hanta Virus

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013442·Hanta Virus - 24 Poly White

FAA Airline - 24 Poly White

FDA UDI
Certified Safety Manufacturing, Inc.·00766588013244·FAA Airline - 24 Poly White

LIPOSUCTION CANNULA

FDA UDI
SONTEC INSTRUMENTS, INC.·B0992013540·LIPOSUCTION CANNULA SPATULATED TIP

FETCH 2 ASPIRATION CATHETER MODEL 109400-001

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEMOGRAPH; OSSTAPLE - ORTHOPEDIC USES FOR SMALL BONE AND FRAGMENT FIXATION FOR THE MEMOGRAPH STAPLE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 27, 2014

SUREFLEX 200 LITHOTRIPSY FIBER

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·June 26, 2013

6800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 3, 2011

ENDEAVOR RX

FDA Adverse Event
Injury ·MEDTRONIC IRELAND·Product code NIQ·January 15, 2014

COREVALVE 26MM AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·September 6, 2016

VISUALASE

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code GEX·December 18, 2020

SOLETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 19, 2014

PLATE,FIXATION,BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HRS·July 25, 2016

ONYX

FDA Adverse Event
Injury ·COVIDIEN (IRVINE)·Product code MFE·May 17, 2017

ONYX

FDA Adverse Event
Death ·COVIDIEN (IRVINE)·Product code MFE·May 17, 2017

MARATHON MICROCATHETER

FDA Adverse Event
Death ·COVIDIEN (IRVINE)·Product code KRA·May 17, 2017

MARATHON MICROCATHETER

FDA Adverse Event
Injury ·COVIDIEN (IRVINE)·Product code KRA·May 17, 2017