10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Trevo XP ProVue Retriever (6X25mm)
FDA 510(k)
FDA Class 2
·Cardiovascular
Manhattan Forceps
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896112919·Manhattan Forceps Angled Tip Titanium
3D Printed Interbody Systems
FDA UDI
Seaspine Orthopedics Corporation·10889981280833·No Profile Spacer, 14x13x7mm, 7 Degree, 3D
MANHATTAN SEVERIN TISSUE FORCEPS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896073685·MANHATTAN SEVERIN TISSUE FORCEPS WITH TYING PLA...
MODIFICATION TO AEQUALIS SHOULDER FRACTURE SYSTEM; AEQUALIS SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ECG PEN
FDA 510(k)
FDA Class 2
·Cardiovascular
IDENTITY XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·January 13, 2014
NEXCARE ABSOLUTE WATERPROOF TAPE
FDA Adverse Event
Injury
·3M CONSUMER HEALTH CARE·Product code KGX·May 24, 2013
QUATTRODE, 30-CM LENGTH PERCUTANEOUS LEAD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 23, 2011
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 4, 2023