255 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.

GLASS LOSS OF RESISTANCE SYRINGE

FDA 510(k)
FDA Class 2 ·Anesthesiology

SOLIDEA

FDA UDI
CALZIFICIO PINELLI SRL·08300496063018·SOCKS FOR YOU BAMBOO OPERA, SIZE XL, GRIGIO, GR...

Bausch + Lomb

FDA UDI
Bausch & Lomb Incorporated·00757770425655·eXTRA TIP FOR N-630 18 GAUGE

Sterilance Press2 Disposable Safety Lancet

FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630115087·

STERiLANCE Press2 Disposable Safety Lancet

FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630131087·

Sterilance Press2 Pressure Activated Safety Lancet

FDA UDI
Sterilance Medical (Suzhou) Inc.·16945630109932·Sterilance Press2 Pressure Activated Safety Lan...

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00840180501337·Medial/Lateral Angled LIF Cobb - 18MM, RIGHT

General Instruments

FDA UDI
ALPHATEC SPINE, INC.·00840180501320·Medial/Lateral Angled LIF Cobb - 18MM, LEFT

TITAN TIBIAL NAIL

FDA 510(k)
FDA Class 2 ·Orthopedic

REAADS ANTI-PHOSPHATIDYLSERINE IGA SEMI-QUANTITIVE TEST KIT

FDA 510(k)
FDA Class 2 ·Immunology

ZILVER 635 SELF-EXPANDING BILIARY STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·August 29, 2022

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·October 8, 2020

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·May 20, 2022

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·June 26, 2024

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·July 1, 2020

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FGE·January 17, 2022

ZILVER 635 BILIARY SELF EXPANDING METAL STENT

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code NIU·November 8, 2019

AUTOPULSE RESUSCITATION SYSTEM MODEL 100

FDA Adverse Event
Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·March 26, 2013

INTEGRIS H5000F/ALLURA 9F

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code IZI·March 21, 2011

MANUAL ORTHOPEDIC SURGICAL INSTRUMENT

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code LXH·June 19, 2008