35 results · 22ms · Sources: EU EUDAMED, US FDA

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BIOPINCE ULTRA FULL CORE BIOPSY INSTRUMENT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

Endo Carry-On Procedure Kit

FDA UDI
MEDIVATORS INC.·00677964069192·Endo Carry-On Procedure Kit

Endeavour™ TruColor™

FDA UDI
METREX RESEARCH, LLC·00810210820257·Endeavour™ TruColor™ headlight system - North A...

Sklar®

FDA UDI
SKLAR CORPORATION·10649111002854·E-Z LOCK INSTR STRINGER 5X12"

Drill Stopper for Long L10 1832

FDA UDI
ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157270·

VANGUARD REPROCESSED FEMORAL COMPRESSION DEVICE

FDA 510(k)
FDA Class 2 ·Cardiovascular

PARADIGM SOF-SET ULTIMATE QR, MODELS 317 AND 318

FDA 510(k)
FDA Class 2 ·General Hospital

Drill Stopper for Long L15/Short L10 1832

FDA UDI
ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157300·

Widex

FDA UDI
Widex A/S·05706069721980·Widex D-FS BTE (Titan grey S-330 ) Telecoil, RC...

Widex

FDA UDI
Widex A/S·05706069720891·Widex UNIQUE U-PA BTE (Titan grey S-330 ) RC coil

Widex

FDA UDI
Widex A/S·05706069722406·Widex D-PA BTE (Titan grey S-330 ) RC coil

Widex

FDA UDI
Widex A/S·05706069722734·Widex CLEAR330 C3-FS BTE (Titan grey S-330 ) Te...

Widex

FDA UDI
Widex A/S·05706069721171·Widex BEYOND B-F2 (Titan grey S-330 ) Telecoil,...

Widex

FDA UDI
Widex A/S·05706069721669·Widex UNIQUE U-FS BTE (Titan grey S-330 ) Telec...

BD TRIAC CENTRIFUGE

FDA Adverse Event
Malfunction ·THE DRUCKER COMPANY·Product code GKG·May 1, 2013

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 10, 2011

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·August 6, 2008

COREVALVE TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·December 23, 2018

THROMBUSTER II

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code MMY·March 17, 2014

THROMBUSTER II

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code DXE·October 23, 2012