30 results · 21ms · Sources: EU EUDAMED, US FDA

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EYEREVE (hioxifilcon D) Soft (hydrophilic) Contact Lens for Daily Wear

FDA 510(k)
FDA Class 2 ·Ophthalmic

OSS™ Orthopedic Salvage System

FDA UDI
Biomet Orthopedics, LLC·00880304554740·

Ceramco® II Silver™

FDA UDI
Dentsply International Inc.·D0011611240·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694036214·2.4mm Cannulated Screwdriver Shaft, Manual

Symmetry Rochester-Pean

FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482040324·Symmetry® Forceps, Rochester-Pean Hemostatic, C...

ZEUS-L

FDA UDI
SPINAL ELEMENTS·00840916141936·ZEUS®-L 10mm Straight Osteotome

Sentry

FDA UDI
Life Spine, Inc.·00190837071189·Set Screw Driver

Scorpio

FDA UDI
Howmedica Osteonics Corp.·07613154020775·Cruciate Retaining Tibial Insert

ARTHREX MIXING AND DELIVERY SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

ORTHOPEDIC SOURCE PRESS-FIT HIP

FDA 510(k)
FDA Class 2 ·Orthopedic

SURESTEP ORIGINAL

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·March 22, 2002

VIDAS® ESTRADIOL II

FDA Adverse Event
Malfunction ·BIOMERIEUX SA·Product code CHP·July 5, 2016

INTERSTIM

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·July 6, 2017

ANGEL SYSTEM WITH ASPIRATION KIT W/ ACDA

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·March 5, 2019

OSS AVL TIBIAL LOCK RING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 14, 2026

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

INFINITI VISION SYSTEM

FDA Adverse Event
Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·June 17, 2011

TEMPORARY CARDIAC PACING WIRE

FDA Adverse Event
ETHICON, INC.·Product code LDF·September 5, 2008

ARTHREX ANGEL SYSTEM WITH ASPIRATION KIT

FDA Adverse Event
Injury ·ARTHREX, INC.·Product code ORG·May 1, 2019

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·January 3, 2013