56 results · 26ms · 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.

HM SURGICAL DRAPES HM SURGICAL EQUIPMENT COVER

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

SPIFE IFE Multi-Channel Pipette

FDA UDI
HELENA LABORATORIES CORPORATION·M52511220000·

TIGER Spine System

FDA UDI
CORELINK LLC·M7256122000·5500 SERIES CONNECTOR - LEFT OFFSET, MONO-AXIA...

IC PROFILER-MR

FDA UDI
SUN NUCLEAR CORP.·05060608880768·Radiation therapy QA device.

IC PROFILER

FDA UDI
SUN NUCLEAR CORP.·05060608880751·Radiation therapy QA device.

EXPERT - Joint Fixation System

FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258638850·EXPERT Knotless Round Plate Ø6.5mm (1un) Rectan...

Electro Lavage

FDA UDI
MECTRA LABS, INC.·00817984010501·Electro Lavage J Hook Dual Spike

Liberty SI

FDA UDI
Spinal Simplicity, LLC·M9431001220000·Lateral SI Joint Fusion Implant 10mm Size C

JOBST Elvarex

FDA UDI
BSN-Jobst GmbH·04019702597837·ELVAREX 2/KNEE HIGH/CLOSED TOE/SOFTFIT/GREY

POURCHEZ RETRO TWIN LUMEN CHRONIC HEMODIALYSIS CATHETER WITH SEPARATED TIPS (WITH AND WITHOUT SIDE HOLES)

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

IMAGYS

FDA 510(k)
FDA Class 2 ·Radiology

INSTRUMENT MANAGER

FDA Adverse Event
Malfunction ·DATA INNOVATIONS, LLC·Product code OUG·December 2, 2022

INSTRUMENT MANAGER SOFTWARE

FDA Adverse Event
Malfunction ·DATA INNOVATIONS LLC·Product code JQP·November 8, 2022

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·December 18, 2015

CAPSUREFIX NOVUS

FDA Adverse Event
Death ·MPRI·Product code DTB·May 21, 2013

ACCU-CHEK ® AVIVA TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·June 13, 2011

AED PLUS

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·August 13, 2008

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MHY·August 31, 2016

ALINITY I PROCESSING MODULE

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code JJE·September 13, 2023

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·December 18, 2015