12 results
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19ms
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Sources: EU EUDAMED, US FDA
FORTE US
FDA 510(k)
FDA Class 2
·Physical Medicine
FIXOS
FDA UDI
Stryker GmbH·07613327095128·Upper Tray Foot & Ankle
Reef TA
FDA UDI
Seaspine Orthopedics Corporation·10889981195564·Interbody, 9mm x 40mm x 18mm, 0 deg
Reef TH
FDA UDI
Seaspine Orthopedics Corporation·10889981203559·Interbody, 9mm x 40mm x 18mm, 0 deg
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955937132·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938306·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939471·Percutaneous Transluminal Angioplasty Balloon C...
Orthopeasia Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
CONTINUM V
FDA 510(k)
FDA Class 2
·Dental
TERUMO CDI 540 CALIBRATOR
FDA Adverse Event
Malfunction
·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DRY·December 23, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013
UNK MAMMARY IMPLANT
FDA Adverse Event
Injury
·ALLERGAN·Product code FWM·March 21, 2014