19 results
·
27ms
·
Sources: EU EUDAMED, US FDA
9.5 FR SIDEWINDER DL INTRA-AORTIC BALLON CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
PARALLEL Y-PIECE, 22MM
FDA UDI
Intersurgical Incorporated·05030267056347·PARALLEL Y-PIECE, 22MM
Mammosite Cavity Evaluation Device Kit (CED)
FDA UDI
Hologic, Inc.·15420045505018·MCEDII TRAY, POST-STERILE
Eye Shield
FDA UDI
KATENA PRODUCTS, INC.·00841668111123·FOX EYE SHIELD ALUMINUM
TITAN™
FDA UDI
Ascension Orthopedics, Inc.·10381780258346·Central Anti-Rotation Peg
Titan™
FDA UDI
Ascension Orthopedics, Inc.·10381780355960·Titan™ Modular Shoulder System Fin-Lock™ Glenoi...
Titan Modular Shoulder System 2.5
FDA UDI
Smith & Nephew, Inc.·00885556860717·GLENOID IMPACTOR HANDLE
Titan Modular Shoulder System 2.5
FDA UDI
Smith & Nephew, Inc.·00885556861547·CENTRAL ANTI-ROTATION PEG
SONACARE SOUND MASSAGER
FDA 510(k)
FDA Class 1
·Physical Medicine
DAB DETECTION KIT
FDA 510(k)
FDA Class 2
·Immunology
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 23, 2013
SIGMA 100 S
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·December 14, 2010
TENDRIL STS
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014
PROWLER SELECT
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code QJP·January 12, 2026
CERENOVUS ENTERPRISE
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code NJE·March 31, 2026
CERENOVUS ENTERPRISE
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code NJE·January 12, 2026
CERENOVUS ENTERPRISE
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code NJE·March 9, 2026
PROWLER SELECT
FDA Adverse Event
Malfunction
·MEDOS INTERNATIONAL SARL·Product code QJP·March 31, 2026
BIOMET StageOne Hip Cement Spacer Mold with Insert, 64 MM, Silicone, Sterile, Item 431185.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020