53 results · 38ms · 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.

Visi Mobile Monitoring System, Visi Mobile Chest Sensor

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772814244·GENUMEDI PT SILVER L VII

CARDIOFAX CE, MODEL PEA-1110K

FDA 510(k)
FDA Class 2 ·Cardiovascular

MEDICAL MAGGOTS, LESOC

FDA 510(k)
FDA Unclassified ·Unknown

FLEXOR RTPS GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·February 27, 2020

QUADRA P FEMORAL STEMS

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 26, 2023

BALL HEADS: BIPOLAR HEAD Ø28X51

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWY·April 7, 2022

ARTICULEZE M HEAD 36MM +1.5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·June 3, 2013

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 30, 2014

UNKNOWN DEPUY INSERT

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·June 23, 2011

90 DEGREE CONTRA ANGLE SCREWDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·March 6, 2017

90 DEGREE CONTRA ANGLE SCREWDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·December 1, 2016

BIOMET MICROFIXATION FACIAL PLATING SYSTEM

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 25, 2017

90 DEG CONTRA ANGLE SCREWDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·October 14, 2016

MECTACER BIOLOX DELTA FEMORAL BALL HEAD

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 18, 2025

90 DEGREE CONTRA ANGLE SCREWDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·October 21, 2016

BIOMNET MICROFIXATION FACIAL PLATING SYSTEM

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·September 23, 2016

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 29, 2020

BIOMET MICROFIXATION FACIAL PLATING SYSTEM

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·March 20, 2017

BIOMET MICROFIXATION FACIAL PLATING SYSTEM

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 12, 2017