17 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SLENDERTONE SYSTEM ABS, MODELS 390, E10, X10; SLENDERTONE SYSTEM SHORTS, MODELS 390, E20
FDA 510(k)
FDA Class 2
·Physical Medicine
MAS PLIF
FDA UDI
Nuvasive, Inc.·00887517204073·MAS PLIF Insulator, Drill/Tap
MP Vial Adapter 13 mm
FDA UDI
WEST PHARMA. SERVICES IL, . LTD·07290108240139·Vial Adapter 13mm FLL SIL - VF
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108697537·Implant Body Try-In Kit
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306802065·Rochester Pean Hemostatic Forceps, Curved, 20cm
OCO DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
MIDAS TOUCH LATEX EXAMINATION GLOVES-POWDER FREE
FDA 510(k)
FDA Class 1
·General Hospital
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·October 30, 2014
SPECTRA WAVEWRITER
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 3, 2020
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·September 14, 2017
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 10, 2018
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code FZP·April 22, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·April 21, 2011
SYNCHROMED II
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·July 3, 2008
MP VIAL ADAPTER 13MM
FDA Adverse Event
Malfunction
·WEST PHARMA. SERVICES IL, LTD·Product code LHI·August 31, 2023
VERTEX RECONSTRUCTION SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·April 27, 2020