15 results · 34ms · 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.

ENDOMEDIX Y-ADAPTER

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

SeaSpine Spacer System - Hollywood

FDA UDI
Seaspine Orthopedics Corporation·10889981090012·Hollywood Angled Inserter

PCA (R) TIBIAL BONE WEDGES

FDA 510(k)
FDA Class 2 ·Orthopedic

OP-CON SURG. INSTRUMENT #10

FDA 510(k)
FDA Class 1 ·Neurology

CHAMBER COMPLETE AUTOFEED 900

FDA Adverse Event
Malfunction ·Product code BTT·May 5, 2021

CHAMBER COMPLETE AUTOFEED 900

FDA Adverse Event
Malfunction ·Product code BTT·January 21, 2020

9800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

NEXGEN MIS TOTAL STEMMED TIBIAL COMPONENT

FDA Adverse Event
Malfunction ·ZIMMER INC·Product code JWH·December 8, 2010

NATURALYTE

FDA Adverse Event
Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

VENTED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 17, 2023

VENTED AUTOFEED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 20, 2023

VENTED AUTOFEED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 23, 2024

CHAMBER COMPLETE AUTOFEED 900

FDA Adverse Event
Malfunction ·Product code BTT·June 3, 2021

FISHER & PAYKEL HEALTHCARE

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 15, 2024

CHAMBER COMPLETE AUTOFEED 900

FDA Adverse Event
Malfunction ·Product code BTT·February 4, 2021