18 results · 21ms · 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.

LATEX EXAMINATION GLOVES, POWDERED

FDA 510(k)
FDA Class 1 ·General Hospital

FLEXMEDICS NITINOL ARCH WIRE

FDA 510(k)
FDA Class 1 ·Dental

RESONANCE METALLIC URETERAL STENT

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·December 13, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 31, 2018

9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 7, 2014

ANIMAS INSULIN CARTRIDGE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·February 15, 2013

AMENDIA GUIDEWIRE

FDA Adverse Event
Malfunction ·AMENDIA, INC.·Product code DQX·January 12, 2011

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 6, 2023

RESONANCE STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·July 25, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·May 29, 2015

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·October 11, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·November 22, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·September 27, 2023

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·August 13, 2018

RESONANCE STENT SET

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·September 12, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·August 16, 2018

RESONANCE STENT SET

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code FAD·January 22, 2019