33 results · 21ms · Sources: EU EUDAMED, US FDA

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PURITAN-BENNETT 700 RENAISSANCE II SPIROMETRY SYSTEM

FDA 510(k)
FDA Class 2 ·Anesthesiology

OCTAGON Infinity BL RC Abutment angled 18° GH 1.5 mm

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50221031·BL RC Abutment angled 18° GH 1.5 mm for OCTAGON...

Millennium

FDA UDI
Avalign Technologies, Inc.·00190776200732·BiManual G Curved single port aspir

Aztec

FDA UDI
Aztecmed/Ent LLC·B87110221030·Bowman Lachrymal Probes, malleable sterling sil...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM

TECHLEM MEDICAL CORP.

FDA registration
TECHLEM MEDICAL CORP.·1 product·🇨🇦 Canada

SIMPLICITY SPINAL SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BANDVIEW SYSTEM

FDA 510(k)
FDA Class 2 ·Hematology

8022103-1997-00001

FDA Adverse Event
Malfunction ·Product code KCT·December 30, 1997

CADD EXTENSION SET

FDA Adverse Event
Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·November 25, 2024

DINAMAP PROCARE SERIES MONITOR

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code MWI·September 9, 2010

DINAMAP PROCARE SERIES MONITOR

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code MHX·September 9, 2010

UNKNOWN SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HWC·April 18, 2022

UNKNOWN SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code HWC·April 18, 2022

UNKNOWN SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·April 18, 2022

BLOOD PUMP PU VALVES 30 ML, IN/OUT Ø9 MM

FDA Adverse Event
Injury ·BERLIN HEART GMBH·Product code DSQ·February 3, 2022

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·March 26, 2013

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·February 28, 2011

XPERT SELF-EXPANDING TRANSHEPATIC BILLIARY STENT SYSTEM

FDA Adverse Event
Malfunction ·ABBOTT VASCULAR SWITZERLAND·Product code FGE·March 25, 2008

UNKNOWN CERAMIC LINER

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·February 24, 2022