25 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Noveos Immunoanalyzer System, Noveos Specific IgE (slgE), Capture Reagent D002, Dermatophagoides farinae
FDA 510(k)
FDA Class 2
·Immunology
Symetri Clear
FDA UDI
ORMCO CORPORATION·00889989082968·U4&5 UNIV SYMETRI CLEAR MCLAUGHLIN, BENNETT & T...
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690199120·AK3 Congruent Insert Trial Size 5, 10mm
DISPOSABLE EYE BLADES
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896019638·DISPOSABLE EYE BLADES #64
Life Instruments
FDA UDI
Life Instrument Corporation·M930719151000·Down Pushing Curette
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915100C0·Custom Down Pusher Curette 30 Degree Angle
Life Instruments
FDA UDI
Life Instrument Corporation·M930719151030·Down Pushing Curette Lat Angle
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915100SC0·Custom Down Pushing Curette 7" handle
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915103S0·Down Pushing Curette (7" Handle) with Lateral Ang
Life Instruments
FDA UDI
Life Instrument Corporation·M93071915100S0·Down Pushing Curette 7" handle
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973107798·TRIAL 90-SRK-191510 POLY-MPCS 5X10 RIGHT
Compression Staple System
FDA UDI
TORNIER, INC.·00846832058754·Staple
WALLFLEX ESOPHAGEAL FULLY COVERED STENT SYSTEM, MODELS M00516700, M00516710, M00516720, M00516730
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FRACTIONAL SKIN RESURFACING (FSR) APPLICATOR
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Life Instruments
FDA UDI
Life Instrument Corporation·M93051915100S10·PSTS-000107 Down Pushing Curette 15"
WALLFLEX ESOPHAGEAL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code ESW·January 23, 2025
WALLFLEX ESOPHAGEAL
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code ESW·February 14, 2025
2800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·July 27, 2011
RESTORE ULTRA
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 26, 2013
ACCURUS 400VS
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·September 26, 2008