12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CLOSED SWABABLE STOPCOCK AND MINIMAL RESIDUAL VOLUME LUER-ACTIVATED SWABABLE-STOPCOCK
FDA 510(k)
FDA Class 2
·General Hospital
Mini-Mono® Brackets
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70602311·Mini-Mono-Brackets Andrews 'N' .018" 200 Brackets
Marina Medical
FDA UDI
MARINA MEDICAL INSTRUMENTS, INC.·00840306811180·Potts-Smith Forceps, 1x2, 21cm
PROTOS DR/CLS
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DXY·November 3, 2006
SELOX ST 53
FDA Adverse Event
Injury
·BIOTRONIK GMBH CO.·Product code DTB·November 3, 2006
JK GLOVES PRE-POWDERED LATEX EXAMINATION GLOVE
FDA 510(k)
FDA Class 1
·General Hospital
TRIAGE BNP CALIBRATION VERIFICATION CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
QUATTRODE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 10, 2013
LIGHTSHEER DUET
FDA Adverse Event
Injury
·LUMENIS, INC.·Product code GEX·April 15, 2011
HYDRATOME RX SHINCTEROTOME
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code KNS·June 12, 2008
CONFIDA BRECKER CURVE GUIDEWIRE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DQX·June 5, 2025
MR Coils The MR Coil is intended to be used in conjunction with a Magnetic Resonance Scanner to produce diagnostic images of the anatomy of interest that can be interpreted by a trained physician.
FDA Enforcement
Class III
·Terminated·Invivo Corporation·October 28, 2020