25 results · 22ms · Sources: EU EUDAMED, US FDA

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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