18 results
·
23ms
·
Sources: EU EUDAMED, US FDA
KWICK KOOLER
FDA 510(k)
FDA Class 1
·Physical Medicine
Kanso® Battery Cover
FDA UDI
COCHLEAR LIMITED·09321502035811·Sandy Blonde
NA
FDA UDI
KEY SURGICAL, INC.·10849771049927·Steinmann Pins, Single diamond, round end, 5/64...
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·14026704912435·
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293784·
Duo Lumbar Interbody Fusion Device
FDA 510(k)
FDA Class 2
·Orthopedic
VISIONS PV 8.2 INTRAVASCULAR ULTRASOUND IMAGING CATHETER, MODEL 88900
FDA 510(k)
FDA Class 2
·Cardiovascular
MECHANICAL (MANUAL) WHEELCHAIR
FDA Adverse Event
Malfunction
·INVAMEX·Product code IOR·April 24, 2014
SIG PS CEM FEM W/LUGS LT SZ4
FDA Adverse Event
Injury
·DEPUY RAYNHAM·Product code JWH·October 4, 2012
SCREW, CORTICAL FIX, POLYAXIAL, MIS 5.5, TI, 6X35MM
FDA Adverse Event
Injury
·DEPUY SYNTHES SPINE·Product code NKB·May 14, 2015
ONCOLOGY SALVAGE SYSTEM - OSS TIBIAL BUSHING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·April 26, 2017
ONCOLOGY SALVAGE SYSTEM - OSS FEMORAL BUSHINGS QTY. 2
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·April 26, 2017
ONCOLOGY SALVAGE SYSTEM - OSS AXLE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·April 26, 2017
ONCOLOGY SALVAGE SYSTEM - OSS 18MM TIBIAL BEARING
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDI·April 26, 2017
ORTHOPEDIC SALVAGE SYSTEM- OSS YOKE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KRO·April 26, 2017
M2A-MAGNUM PF CUP 50ODX44ID
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2022
MLRY-HD POR FMRL 9X150MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·November 4, 2022
Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty
FDA Enforcement
Class II
·Ongoing·Exactech, Inc.·April 10, 2024