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