14 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
PENEVAC ABC HANDPIECE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BASE
FDA UDI
Nuvasive, Inc.·00887517701701·BASE HL Trial, 10x38x28mm 20°
ReLine
FDA UDI
Nuvasive, Inc.·00195377075116·RELINE C Screw, 5.0x20mm Cort Canc
Zuma™
FDA UDI
Seaspine Orthopedics Corporation·10889981037543·Plate Trial, 20mm. Zuma™ Trials are used to det...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937392·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939730·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938566·Percutaneous Transluminal Angioplasty Balloon C...
AlphaVent
FDA UDI
STRYKER CORPORATION·07613327563078·ALPHAVENT SUTURE ANCHOR 5.5MM PEEK, SUTURE ANCH...
SLIDEX STREPTO-KIT
FDA 510(k)
FDA Class 1
·Microbiology
MEDICAL DYNAMICS CCD SOLID STATE VIDEO CAMERA 5930
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
ZMR®
FDA UDI
Zimmer, Inc.·00889024157828·
SYSTEM 6 ASEPTIC HOUSING ASSY
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code KIJ·February 11, 2013
TAPERLOC POR LAT FMRL 12.5X145
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code LPH·July 24, 2014
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011