10 results · 25ms · 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.

BIOTRACK MONITOR (BIOTRACK REAGENT CARTRIDGES)

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

Shoreline ACS

FDA UDI
Seaspine Orthopedics Corporation·10889981162542·Drill, 20mm

Carriere Motion Clear Class II

FDA 510(k)
FDA Class 2 ·Dental

CURATIVE DENTAL ACRYLIC TEETH

FDA 510(k)
FDA Class 2 ·Dental

INSYNC III

FDA Adverse Event
Injury ·IPG MFG SWITZERLAND·Product code LWP·June 10, 2014

TOTALCARE BED

FDA Adverse Event
Malfunction ·HILL-ROM, INC.·Product code FNL·October 29, 2012

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 22, 2015

RIGIDFIX FEM 3.3MM S/T XPIN

FDA Adverse Event
Malfunction ·DEPUY MITEK LLC US·Product code HTY·January 21, 2019

OEC 6800 Miniview, Image-intensified fluoroscopic x-ray system used during diagnostic, surgical and interventional procedures. Designed to provide the physician with general fluoroscopic visualization of the patient including but not limited to surgical orthopedic and extremity imagine. The device is not intended for whole-body pediatric imaging.

FDA Enforcement
Class I ·Terminated·GE OEC Medical Systems, Inc·August 1, 2012

DATEX-OHMEDA S/5 SINGLE-WIDTH AIRWAY MODULE, E-MINIC AND ACCESSORIES. DATEX-OHMEDA S/5TM FM WITH L-FICU04 ANDL-FICUO4A SOFTWARE AND N-FCREC MODULE **(OUS only). E-miniC and accessories is indicated for monitoring C02 and respiration rate of all hospital patients.

FDA Enforcement
Class I ·Terminated·GE Healthcare, LLC·July 30, 2014