17 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.

Patient Monitor

FDA 510(k)
FDA Class 2 ·Cardiovascular

PLAYTEX SPORT PLASTIC, PLAYTEX SPORT PLASTIC MULTIPACK TAMPONS

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

UNITED STEM, PSA TYPE

FDA 510(k)
FDA Class 2 ·Orthopedic

KYPHON HV-R BONE CEMENT

FDA Adverse Event
Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 25, 2017

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·April 7, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 19, 2020

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 4, 2019

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Injury ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 17, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·December 17, 2018

KYPHX® HV-R¿ BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·February 7, 2017

OSSIX BONE, OSSIX PLUS

FDA Adverse Event
Injury ·DATUM DENTAL LTD.·Product code NPM·June 22, 2022

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·October 12, 2017

KYPHX HV-R BONE CEMENT

FDA Adverse Event
Malfunction ·MDT KYPHON NEUCHATEL MFG·Product code NDN·July 9, 2020

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MPRI·Product code LWS·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Malfunction ·WAVELIGHT GMBH·Product code LZS·June 16, 2011

MOZEC¿ NC RX PTCA BALLOON DILATATION CATHETER

FDA Adverse Event
Malfunction ·MERIL LIFE SCIENCES PRIVATE LIMITED·Product code LOX·December 13, 2022