50 results · 23ms · Sources: EU EUDAMED, US FDA

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ELITE + LASER SYSTEM

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

Novo Surgical Inc.

FDA UDI
NOVO SURGICAL, INC.·00842331159190·operating scissors, blunt/blunt, curved, 5 3/4"...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L141425120·14mm H x 14mm W x 25mm L XLIF Trial 12 degree L...

TALOS° HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321414250·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311414250·

TALOS®-A

FDA UDI
SpineArt SA·07640375237811·TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D26 ...

CONSERVE PLUS REVISION SHELL AND CONSERVE PLUS THICK SHELL

FDA 510(k)
FDA Class 3 ·Orthopedic

MICROSCAN DRIED GRAM-NEGATIVE MIC/COMBO PANEL, B1017 PANEL SERIES

FDA 510(k)
FDA Class 2 ·Microbiology

TIBIAL INSERT FIXED SPHERE FLEX #5/13 MM R

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 29, 2018

GMK-SPHERE TIBIAL INSERT FIXED SPHERE FLEX SIZE 5/13 MM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 3, 2019

CART 9733856 S7 STAFF ASSEMBLED 110V

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019

CONSULTA CRT-D

FDA Adverse Event
Death ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·June 3, 2013

TOTAL ASR FEM IMP SIZE 51

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 22, 2011

ACCU-CHEK ACTIVE TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·September 3, 2008

GMK SPHERE TIBIAL INSERT SIZE 5/13 MM RIGHT

FDA Adverse Event
Injury ·Product code JWH·July 17, 2015

HF UNIT "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·April 23, 2021

HF UNIT "ESG-400"

FDA Adverse Event
Injury ·OLYMPUS WINTER & IBE GMBH·Product code GEI·December 5, 2017

HF UNIT "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·July 8, 2020

HF UNIT "ESG-400"

FDA Adverse Event
Malfunction ·OLYMPUS WINTER & IBE GMBH·Product code GEI·November 17, 2020

STEALTHSTATION® S7´

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·June 20, 2019