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

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Radionuclide Radiation Therapy System Product The product is a teletherapy device intended for stereotactic irradiation of head structures ranging from very small target sizes of a few millimeters to several centimeters.

FDA Enforcement
Class II ·Terminated·Elekta, Inc.·May 4, 2016

Abiomed Introducer Kit, 23 Fr, w/Hlx Vlv Sterile Individual, and Part of Pump Set (004334, 0046-0035, 0052-0002) Part Number: 0052-3021. Intended for introduction of the Impella Catheter into the body

FDA Enforcement
Class II ·Ongoing·Abiomed, Inc.·January 17, 2024

HeartWare Ventricular Assist System Controller Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HVAD is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter

FDA Enforcement
Class I ·Terminated·Heartware, Inc.·October 26, 2016

BYTE Aligner System REF PRS-0063 BYTE All-Day Aligner System BYTE AT-Night Aligner System A custom-made orthodontic appliance, typically supplied in series intended to be worn in succession and self-changed every few weeks, designed to influence the shape and/or function of the stomatognathic system to correct malocclusions.

FDA Enforcement
Class II ·Ongoing·Straight Smile, LLC·January 1, 2025

HeartWare Ventricular Assist System (HeartWare Controller) Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare System is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

FDA Enforcement
Class I ·Terminated·HeartWare Inc·March 4, 2015

HeartWare HVAD Pump Implant Kit (Heartware Ventricular Assist Device) - HeartWare Battery For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage ventricular heart failure.The HeartWare VAS is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

FDA Enforcement
Class II ·Terminated·HeartWare Inc·May 21, 2014

HeartWare Ventricular Assist System (HVAD), US product: Model No.: 1103; and International Product: Model No.: 1104XX. Product Usage: For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. Designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

FDA Enforcement
Class I ·Ongoing·HeartWare, Inc·October 19, 2016

daVinci Harmonic ACE Curved Shears

FDA Enforcement
Class II ·Ongoing·Intuitive Surgical, Inc.·February 27, 2019

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001U.

FDA Enforcement
Class II ·Ongoing·MEDLINE INDUSTRIES, LP - Northfield·October 16, 2024

MEDLINE Automatic Digital Blood Pressure Monitor, REF MDS1001UT.

FDA Enforcement
Class II ·Ongoing·MEDLINE INDUSTRIES, LP - Northfield·October 16, 2024

MEDLINE AUTOMATIC DIGITAL BLOOD PRESSURE UNIT, REF MDS1001

FDA Enforcement
Class II ·Ongoing·MEDLINE INDUSTRIES, LP - Northfield·October 16, 2024

Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device) Catalog Numbers: 1100, 1101, 1102, 1103, 1104, and 1205. For use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare VAS is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter.

FDA Enforcement
Class I ·Terminated·HeartWare Inc·April 30, 2014

HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a bridge-to-cardiac transplantation in patients who are at risk of death from refractory end-stage left ventricular heart failure. The HeartWare Ventricular Assist System (VAS) is designed for in-hospital and out-of-hospital settings, including transportation via fix-wing aircraft or helicopter

FDA Enforcement
Class I ·Ongoing·Heartware·May 3, 2017

K2M, ALEUTIAN Interbody Spacer Systems, EN AN Lordotic Spreader, Stainless Steel, Non-Sterile, Qty 1, Catalog # 5203-90179, UDI # 10888857108929, Size 28x6mm, 18 Product Usage: Used to simulate the height of the cage and expand the spine disc space to determine the optimal implant size base on patient anatomy.

FDA Enforcement
Class II ·Terminated·K2M, Inc·May 27, 2020

Ventilator Tubing

FDA Enforcement
Class II ·Terminated·Instrumentation Industries Inc·November 18, 2015

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Catheter, 6", Part Number 2110-0503 Product Usage: Facilitate placement of bone cement in weakened or diminished bone

FDA Enforcement
Class II ·Terminated·Orthovita, Inc., dBA Stryker Orthobiologics.·June 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger, 8", Part Number 2110-0502 Product Usage: Facilitate placement of bone cement in weakened or diminished bone

FDA Enforcement
Class II ·Terminated·Orthovita, Inc., dBA Stryker Orthobiologics.·June 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Plunger Delivery System, 6", Part Number 2090-0505 Product Usage: Facilitate placement of bone cement in weakened or diminished bone

FDA Enforcement
Class II ·Terminated·Orthovita, Inc., dBA Stryker Orthobiologics.·June 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Catheter, 8", Part Number 2110-0526 Product Usage: Facilitate placement of bone cement in weakened or diminished bone

FDA Enforcement
Class II ·Terminated·Orthovita, Inc., dBA Stryker Orthobiologics.·June 5, 2013

Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Syringe Delivery System, 6", Part Number 2090-0504 Product Usage: Facilitate placement of bone cement in weakened or diminished bone

FDA Enforcement
Class II ·Terminated·Orthovita, Inc., dBA Stryker Orthobiologics.·June 5, 2013