108 results · 60ms · 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.

THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)

FDA Adverse Event
Malfunction ·RENOVO, INC.·Product code NLM·April 5, 2021

THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)

FDA Adverse Event
Malfunction ·RENOVO, INC.·Product code NLM·April 5, 2021

ARTHROSCOPIC SHAVER, TORPEDO REGULAR LENGTH LIME GREEN

FDA Adverse Event
Malfunction ·RENOVO, INC.·Product code NLM·April 5, 2021

THREADED CANNULA W/OBTURATOR (TRANSLUCENT, PURPLE)

FDA Adverse Event
Malfunction ·RENOVO, INC.·Product code NLM·April 5, 2021

DYONICS ACROMIOBLASTER

FDA Adverse Event
Injury ·RENOVO, INC.·Product code HRX·May 19, 2026

DENOVO SPACE MAINTAINER BAND CHAIRSIDE SPACE MAINTAINER

FDA Adverse Event
Injury ·DENOVO DENTAL, INC.·Product code ECM·September 1, 2022

S 150 STAND-ALONE ANTERIOR CERVICAL INTERBODY FUSION

FDA Adverse Event
Malfunction ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code OVE·March 22, 2017

TESERA 3-D PRINTED ALIF CAGE

FDA Adverse Event
Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code MAX·July 3, 2018

A200 KNEE SYSTEM

FDA Adverse Event
Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016

A200 KNEE SYSTEM

FDA Adverse Event
Injury ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code JWH·September 16, 2016

S100

FDA Adverse Event
Malfunction ·RENOVIS SURGICAL TECHNOLOGIES, INC.·Product code KWP·April 12, 2017

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·November 7, 2024

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·May 11, 2021

SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER

FDA Adverse Event
Malfunction ·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 1, 2026

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·March 20, 2023

THERMOCOOL® SMART TOUCH¿ BI-DIRECTIONAL NAVIGATION CATHETER

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·March 18, 2024

IMPELLA 5.5 WITH SMARTASSIST S2 SET, US

FDA Adverse Event
Malfunction ·ABIOMED, INC. - 1220648·Product code OZD·March 18, 2026

IMPELLA 5.5 WITH SMARTASSIST S2 SET, US

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code OZD·March 19, 2026

SHOCKWAVE IVL SYSTEM WITH THE SHOCKWAVE C2+ CORONARY IVL CATHETER

FDA Adverse Event
Injury ·SHOCKWAVE MEDICAL, INC.·Product code QMG·April 24, 2026

KIT, 14FR INTRODUCER, 13CM&25CM, STERILE

FDA Adverse Event
Injury ·ABIOMED, INC. - 1220648·Product code DYB·March 3, 2026