61 results
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26ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Apyx One Console
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00885074362519·SCREW 7221830 HA COATED CANN 8.5 X 30
BD BBL™ Nitrate Broth with Durham Tube
FDA UDI
BECTON, DICKINSON AND COMPANY·30382902218303·BD BBL™ Nitrate Broth with Durham Tube
Meridian
FDA UDI
Seaspine Orthopedics Corporation·10889981247256·No-Profile Interbody, 39mm x 27mm x 18mm, 30 Deg
Linear™ ST
FDA UDI
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·08714729771180·30cm 8 Contact Lead Kit
Linear ST ™
FDA UDI
BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·M365SC2218300·Linear ST, 30cm 8 Contact Lead Kit
ANSER Clavicle Pin
FDA 510(k)
FDA Class 2
·Orthopedic
SORIN BIOMEDICA SMARXT BCD VANGUARD SURFACE MODIFIED CARDIOPLEGIA SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 22, 2012
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 21, 2023
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 16, 2013
PRECISION?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·October 7, 2025
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 26, 2024
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 21, 2021
PRECISION®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 14, 2015
LINEAR ST
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 14, 2023
PRECISION®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·February 24, 2015
PRECISION®
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·December 23, 2013
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·October 3, 2011
ADVIA CENTAUR CA 19-9 ASSAY
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code NIG·November 4, 2008