24 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Force Fiber OrthoTape suture
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ECG Module(AHA)
FDA UDI
SAMSUNG MEDISON CO., LTD.·08806167712532·
AGXO
FDA UDI
Oticon A/S·05707131289254·H110V2 TI, MINIRITE 312 WL SIL AGXO
OSS™ Orthopedic Salvage System
FDA UDI
Biomet Orthopedics, LLC·00880304239593·
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768L15043818K0·Tap
Restore
FDA UDI
KEYSTONE DENTAL, INC.·D768L15043813K0·Tap
Tibial Regular Trial Insert Size 2
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215073848·
STEALTHSTATION SYSTEM UPDATE
FDA 510(k)
FDA Class 2
·Neurology
POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
2027971-2024-150438
FDA Adverse Event
Injury
·NOBEL BIOCARE USA, LLC·Product code DZE·November 29, 2024
CART 9734056 S7 STAFF SHRT 100-120V INTL
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 14, 2019
CART 9733856 S7 STAFF ASSEMBLED 110V
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 4, 2019
NAVLOCK UNIVERSAL GREEN TRACKER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·October 30, 2015
SCREW DRIVER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·August 5, 2019
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013
HEARTSTART MRX -EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·June 8, 2011
SYNCHROMED
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·September 5, 2008
CART 9734056 S7 STAFF SHRT 100-120V INTL
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC·Product code HAW·June 18, 2019
CART 9734056 S7 STAFF SHRT 100-120V INTL
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·May 18, 2018
NAV THORACIC PROBE TIP
FDA Adverse Event
Injury
·MEDTRONIC NAVIGATION, INC.·Product code OLO·August 27, 2014