66 results · 21ms · 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.

ACUSON Juniper Diagnostic Ultrasound System

FDA 510(k)
FDA Class 2 ·Radiology

Pantheon System

FDA UDI
ADLER ORTHO SPA·08050880238323·Pantheon Bridging Collar Ø 30 mm for Stem Ø 13 mm

3.0 RIO® ROBOTIC ARM - MICS

FDA Adverse Event
Malfunction ·MAKO SURGICAL CORP.·Product code OLO·July 16, 2019

TAPERLOC COMPLETE

FDA UDI
Biomet Orthopedics, LLC·00880304480896·

EZ-Stick

FDA UDI
COMPASS HEALTH BRANDS CORP.·00850958007725·1.5"x3.5" Foam

EZ-Stick

FDA UDI
COMPASS HEALTH BRANDS CORP.·10850958007722·1.5"x3.5" Foam, Case of 10

LIGATURE WIRE 30GA .010(4 OZ)

FDA UDI
W.H. Holden, Inc.·D9282011300·

Taperloc® Complete

FDA UDI
Biomet Orthopedics, LLC·00887868508370·

LIPOSUCTION CANNULA

FDA UDI
SONTEC INSTRUMENTS, INC.·B0992011300·LIPOSUCTION CANNULA WITH THREE HOLES STRAIGHT

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197206181·BABY -KOCHER ATRAUMA Intestinal Clamp 130mm,...

Viceroy

FDA UDI
DIOMEDICAL CO.,LTD.·08800113905061·VICEROY Rod - 6.0 (D)6x(L)130mm

3D MANUAL COARSE MANIPULATOR MN-188NE

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

SPECATH CENTRAL VENOUS CATHETER KITS

FDA 510(k)
FDA Class 2 ·General Hospital

HammerTech

FDA UDI
FUSION ORTHOPEDICS, LLC·00852164007889·PEEK Implant Instrument Kit Small

NUTRILINE

FDA Adverse Event
Malfunction ·VYGON USA·Product code LJS·October 25, 2023

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

CONSTELLATION WITH LASER

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 29, 2011

SYNERGY

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code LGW·July 2, 2013

ACRYSOF TORIC

FDA Adverse Event
Other ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·July 28, 2011

GUARDWIRE 200CM W/6F EXPORT XT

FDA Adverse Event
MEDTORNIC, INC·Product code NFA·December 8, 2011