17 results · 20ms · Sources: EU EUDAMED, US FDA

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PLASMAIR, MODEL T2006

FDA 510(k)
FDA Class 2 ·General Hospital

RMO

FDA UDI
Rmo, Inc.·00885797100122·REMOV QUADHELIX KIT

UNIPOLAR NEEDLES

FDA 510(k)
FDA Class 2 ·Anesthesiology

PROLENE (POLYPROPYLENE) 3D PATCH, NONABSORBABLE SYNTHETIC SURGICAL MESH

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

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDIC, INC.·Product code KWP·October 30, 2014

DREAMSTATION AUTO CPAP

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·October 15, 2024

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·March 26, 2025

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·September 14, 2017

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·December 17, 2014

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·January 10, 2018

PERFIX PLUG

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·April 15, 2013

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE

FDA Adverse Event
Injury ·ETHICON, INC.·Product code GAS·April 27, 2011

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·July 3, 2008

VERTEX RECONSTRUCTION SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 27, 2020

ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·August 3, 2022

ARCHITECT SIROLIMUS

FDA Adverse Event
Malfunction ·ABBOTT IRELAND DIAGNOSTICS DIVISION·Product code NRP·February 5, 2026

ABBOTT TUBE EDTA PLH 13X75 2.0 PNK

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·September 17, 2019