31 results · 32ms · Sources: EU EUDAMED, US FDA

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IBD-SCAN

FDA 510(k)
FDA Class 1 ·Immunology

EQUINOXE PRIMARY SHOULDER COMPONENTS

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWS·August 25, 2022

SOFTFORM SOFT TISSUE AUGMENTATION TUBE WITH INSERTION TOOL MODIFICATIONS FOR STRANDS AND SUTURE HOLES

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ENT LASERVISION

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·March 27, 2020

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·June 27, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·February 6, 2019

VIBRANT SOUNDBRIDGE

FDA Adverse Event
Injury ·VIBRANT MED-EL HEARING TECHNOLOGY GMBH·Product code MPV·April 3, 2013

DEXTRUS 4136

FDA Adverse Event
Injury ·BIOTRONIK SE & CO. KG.·Product code NVZ·March 29, 2011

CONTAK RENEWAL

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS, INC·Product code NIK·May 8, 2008

EQUINOXE REVERSE 38MM HUMERAL LINER +0

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 17, 2022

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·June 3, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·July 9, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·October 1, 2021

EQUINOXE, HUMERAL HEAD SHORT, 44MM (ALPHA)

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·July 30, 2019

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·September 3, 2019

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code HSD·September 30, 2024

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 5, 2019

MDLR CNLTD TRIDRV DRVR

FDA Adverse Event
Malfunction ·EXACTECH, INC.·Product code LXH·August 29, 2023