19 results · 27ms · Sources: EU EUDAMED, US FDA

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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