49 results · 27ms · 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.

MAGNETOM Aera and MAGNETOM Skyra with syngo MR E11C - AP02 Software

FDA 510(k)
FDA Class 2 ·Radiology

Archimed 631 Spinal Brace

FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357633128·

Laparoscope

FDA UDI
SOPRO-COMEG GmbH·04059082032313·

Laparoscope

FDA UDI
SOPRO-COMEG GmbH·04059082003849·

Laparoscope

FDA UDI
SOPRO-COMEG GmbH·04059082003832·

Laparoscope

FDA UDI
SOPRO-COMEG GmbH·04059082032306·

N.A.

FDA UDI
DENTAURUM GmbH & Co.KG·J011163312000·ConTec Go! etching gel in syringes

UPD-Y0003

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MODIFICATION TO ATLANTIS SR PRO 2 AND SR PRO CORONARY IMAGING CATHETERS, MODEL 39014 AND 38942

FDA 510(k)
FDA Class 2 ·Cardiovascular

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 3, 2017

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 2, 2017

UNKNOW HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 3, 2017

PDS II POLYDIOXANONE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code NEW·December 3, 2019

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·December 3, 2019

KANEKA PTCA CATHETER CO-R7 (IKAZUCHI ZERO)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LOX·March 17, 2020

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDI·February 2, 2017

UNKNOWN HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code JDG·February 3, 2017

GYNECARE TVT OBURATOR SYSTEM

FDA Adverse Event
Injury ·ETHICON INC.·Product code OTN·June 11, 2013

ALTRUA

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 15, 2011

TOTALCARE BARIATRIC

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·September 9, 2008