57 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SOLOPATH RE-COLLAPSIBLE ACCESS SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
CoRoent
FDA UDI
Nuvasive, Inc.·00887517574381·CoRoent Ant TLIF Ti, 12x11x40mm 4°
Cohere
FDA UDI
Nuvasive, Inc.·00887517013187·COHERE TLIF-O Trial, 12x14mm 4°
Health Support
FDA UDI
Carolon Company·00078301121441·
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515016897·Olsen-Hegar N.H., 5 1/2"
TAPERLOC®
FDA UDI
Biomet Orthopedics, LLC·00880304430730·
SafeGuide®
FDA UDI
DIVERSATEK HEALTHCARE, INC.·10816734021023·Cleaning Adapters
UniTip Catheter
FDA UDI
Unisensor AG·07640172973226·
CONCENTRIC BALLOON GUIDE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
HUIBAO BODY FAT SCALE
FDA 510(k)
FDA Class 2
·Cardiovascular
Ascendant
FDA UDI
Choice Spine, LP·10885862260949·
LINEAR ST
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·June 13, 2023
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 19, 2026
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
3M LOBAN 2 ANTIMICROBIAL DRAPE
FDA Adverse Event
Other
·3M HEALTH CARE·Product code KKX·August 13, 2008
LIFESTENT FLEXSTAR VASCULAR STENT SYSTEM
FDA Adverse Event
Injury
·ANGIOMED GMBH & CO. MEDIZINTECHNIK·Product code NIP·June 7, 2011