1,847 results · 27ms · Sources: EU EUDAMED, US FDA

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TunnelVision Endoscopic Soft Tissue Release System and the HBL Blade Assembly

FDA 510(k)
FDA Class 2 ·Orthopedic

Darby Dental Supply, LLC

FDA UDI
DARBY DENTAL SUPPLY, LLC·00889813525227·DERMASILK NITRILE GLOVE L

Autoimmune EIA

FDA UDI
BIO-RAD LABORATORIES, INC.·00847817018213·Autoimmune EIA Anti-Cardiolipin IgM Test Kit

JAWS Nitinol Staple System

FDA UDI
Paragon 28, Inc.·00889795049926·Straight Staple Assembly, 25 x 20mm

JAWS® Nitinol Staple System

FDA UDI
Paragon 28, Inc.·00889795124234·JAWs Great White Nitinol Staple System, 25 x 20...

Bindex BI-100

FDA 510(k)
FDA Class 2 ·Radiology

HD-550 Video Endoscope System

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

CARTO VIZIGO¿ 8.5F BI-DIRECTIONAL GUIDING SHEATH - SMALL

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code LPB·April 20, 2020

SYNCHROMED II

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LKK·December 4, 2008

MONOCRYL PLUS ANTIBACTERIAL SUTURES

FDA Adverse Event
Malfunction ·ETHICON, INC.·Product code GAN·September 16, 2011

FINELINE II

FDA Adverse Event
Malfunction ·CPI - DEL CARIBE·Product code DTB·July 29, 2013

ALARIS PCU MODULE

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FRN·September 2, 2020

ALARIS PC UNIT

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FRN·September 3, 2020

TBD

FDA Adverse Event
Injury ·SORIN GROUP ITALIA S.R.L.·Product code KRH·September 20, 2020

DREAMSTATION AUTO BIPAP

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·March 31, 2022

ALARIS PUMP MODULE

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·December 2, 2020

HEARTSTART ONSITE

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 2, 2020

FLANGE FIXTURE ST 4MM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·February 24, 2020

ETHICON PHYSIOMESH COMPOSITE MESH 15X20CM OVAL

FDA Adverse Event
Injury ·ETHICON INC.·Product code FTL·April 30, 2020

TACTICATH¿ QUARTZ CONTACT FORCE ABLATION CATHETER, 65MM

FDA Adverse Event
Malfunction ·VENUSA DE MEXICO S.A. DE C.V.·Product code OAE·September 2, 2022