18 results
·
26ms
·
Sources: EU EUDAMED, US FDA
A1CNOW FOR RX HOME USE
FDA 510(k)
FDA Class 2
·Hematology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526743670·ACHIMED ACHILLES SUPP SILVER IV
Midway Select
FDA UDI
MIDWAY DENTAL SUPPLY, LLC·10843717102288·Cover Film 4" x 6" Blue 1200 sht roll
Humelock II Cemented Shoulder System
FDA UDI
FX SOLUTIONS·03701037305768·PUNCHER Ø34mm
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00841036019563·
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037317846·PUNCHER Ø34mm W/ CUT 2.0mm
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037317808·PUNCHER Ø34mm W/ CUT 1.8mm
Biosteon
FDA UDI
STRYKER CORPORATION·07613154111190·23MM BIOSTEON SCREW DRIVER
SPIRAL RADIUS 90-D RODDING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
TELESCOPIC PLATE SPACER THORACOLUMBAR (TPS-TL) SPINAL SYSTEM, MODELS 8123, 8124, 8132, 8133, 8156, 8157, 8158, & 8189
FDA 510(k)
FDA Class 2
·Orthopedic
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROATION KNEE
FDA Adverse Event
Injury
·MATORHTO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Malfunction
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MEDIAL ROTATION KNEE
FDA Adverse Event
Injury
·MATORTHO LIMITED·Product code JWH·January 22, 2016
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
Malfunction
·UNKNOWN·Product code ITJ·March 25, 2013
HEARTMATE II LVAS
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·March 16, 2011
PRECISION XTRA / OPTIUM
FDA Adverse Event
Malfunction
·ABBOTT DIABETES CARE LIMITED UK·Product code NBW·March 26, 2008