15 results · 23ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

LiteWalk

FDA 510(k)
FDA Class 2 ·Physical Medicine

FIDISTM CONNECTIVE 10, FIDISTM ANALYZER, CARIS

FDA 510(k)
FDA Class 2 ·Immunology

AJUST ADJUSTABLE SINGLE INCISION SLING

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 22, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·September 3, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 27, 2025

LASER HAIR GROWTH CAP

FDA Adverse Event
Injury ·UNKNOWN·Product code OAP·February 26, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 12, 2025

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·May 13, 2026

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 22, 2025

2520274-2013-03835

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HRS·June 27, 2013

RELIANT STENT GRAFT BALLOON CATHETER

FDA Adverse Event
Death ·MEDTRONIC CARDIOVASCULAR·Product code DQY·October 8, 2008

M SERIES

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·July 1, 2011

S4 ROD-TO-ROD CONNECTOR REVIS.SCREW DRV.

FDA Adverse Event
Malfunction ·AESCULAP AG·Product code HXX·September 21, 2015

EXPRESS SD RENAL/BILIARY

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 11, 2025