63 results
·
26ms
·
Sources: EU EUDAMED, US FDA
uPMR 790
FDA 510(k)
FDA Class 2
·Radiology
X-CORE
FDA UDI
Nuvasive, Inc.·00887517244383·X-CORE 2 Ti Endcap, Ø16x18x30mm 4°
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304270459·
OsteoMed
FDA UDI
OSTEOMED LLC·00842528128169·3.0 X 14mm Cannulated Headed Screw, T10
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193110738·HA PEEK EVOS Rotate, , 14mmx12mmx 30mm , FLAT 8...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515027091·Adjustable Mastoid Retr, Blunt 6 1/2
MIRADRY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ATLAS SPEEDER HEAD/CERVICAL COIL, MODEL MJAH-137A
FDA 510(k)
FDA Class 2
·Radiology
PINN CAN BONE SCREW 6.5MMX15MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
SUMMIT POR TAPER SZ6 STD OFF
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
PINN CAN BONE SCREW 6.5MMX25MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·August 14, 2018
9600+
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 3, 2008
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011
MTS A/B/D MONOCLONAL AND REVERSE GROUPING CARD
FDA Adverse Event
Malfunction
·MICROTYPING SYSTEMS·Product code KSZ·June 21, 2013
BIOMET CC I-BEAM TRAY 79MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 7, 2018
VNGD CR TIB BRG 12X79/83
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 7, 2018
UNKNOWN PATELLA
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 7, 2018
VANGUARD CR TIBIAL BEARING
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018
BIOMET CC I-BEAM TRAY
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018
VGD CRUC RET TIB BRG 11X79/83
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018