37 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
STERILIZATION CASSETTE
FDA 510(k)
FDA Class 2
·General Hospital
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304000971·
OsteoMed
FDA UDI
OSTEOMED LLC·00842528100103·1.6mm Driver Stem w/Post, Short, Hex
3M™ Unitek™
FDA UDI
3M UNITEK CORPORATION·00652221037770·Unitek(TM) Bicuspid Band General Purpose Narrow...
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321416160·
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613042745·Precision Folding Ear Knife Handle Straight 8mm...
TALOS®-A
FDA UDI
SpineArt SA·07640375237736·TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D26 ...
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973102014·Poly Insert MPCS, Size 6R, 16mm
THE GRAPPLR AND GRAPPLR EXTENDER
FDA 510(k)
FDA Class 2
·Orthopedic
BGRAN SYNTHETIC OSTEOCONDUCTIVE SCAFFOID
FDA 510(k)
FDA Class 2
·Orthopedic
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929063828·Cervical 14Dx16Wx16H
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929064207·Solid 14Dx16Wx16H
TARGET DEVICE GAMMA3 300X160MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·November 13, 2012
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929034897·Corpectomy, 14Dx16Wx16H 0°
Matrixx System
FDA UDI
NEXXT SPINE, LLC·00889929035061·Corpectomy, 14Dx16Wx16H 6°
BIOMET TIBIAL TRAY WITH LOCKING BAR AND SCREW
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 9, 2018
BCM PALACOS UNKNOWN
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·February 9, 2018
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 4, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 3, 2013
REALIZE
FDA Adverse Event
Malfunction
·ETHICON ENDO SURGERY·Product code LTI·June 15, 2011