21 results · 30ms · Sources: EU EUDAMED, US FDA

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VANISHPOINT I.V. CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital

AnastoPod™

FDA UDI
LSI Solutions, Inc.·00850012846260·AnastoPod™ DEVICE

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X0814200·8mm H x 14mm W x 20mm L x 0 degrees XLIF

PMMA disc

FDA UDI
Dentsply International Inc.·D00180814200·

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587L081420120·8mm H x 14mm W x 20mm L XLIF Trial 12 degree Lo...

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X081420120·8mm H x 14mm W x 20mm L x 12 degrees XLIF

Yellowstone

FDA UDI
SUMMIT SPINE LLC·B587X08142080·8mm H x 14mm W x 20mm L x 8 degrees XLIF

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613098971·Cottle Neivert Retractor, Double Ended, 2 Prong...

SUPERLINE

FDA Adverse Event
Injury ·DENTIUM USA·Product code DZE·September 3, 2020

SLIDESCAN

FDA 510(k)
FDA Class 2 ·Hematology

MM-87 MOTOR-DRIVE MANIPULATOR

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·November 4, 2015

TENSION FREE VAGINAL TAPE

FDA Adverse Event
Injury ·ETHICON INC·Product code OTN·April 26, 2013

TRUFILL DCS ORBIT DETACHABLE COILS COMPLEX

FDA Adverse Event
Malfunction ·CORDIS NEUROVASCULAR, INC.·Product code HCG·May 9, 2011

MESA

FDA Adverse Event
Injury ·K2M·Product code MCV·July 24, 2008

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LJT·November 17, 2017

CANNULA & CATHETER

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DWF·April 22, 2025

VITAL-PORT ATTACHED SILICONE CATHETER WITH INT TITANIUM POWER INJECTABLE PORT

FDA Adverse Event
Injury ·COOK VASCULAR INC·Product code LIT·May 23, 2016

GAM Kirschner Wire, Sterile R, T2 K-Wire, Sterile R and T2 K-Wire Recon, Stryker Trauma GmbH, Prof.-Kuntscher-Strasse 1-5, Schonkirchen, Germany 24232; T2 K-Wire, Sterile R Intended for the temporary stabilization of bone segments or fragments

FDA Enforcement
Class II ·Terminated·Stryker Howmedica Osteonics Corp.·December 28, 2016

Alaris Syringe Pump, Model No. 8110. Delivers fluids. Expansion of Affected Units: BOM Housing Assembly Service, Part No. 49000226, and Lower Housing/Carriage Block Assembly, Part No. 148188-100.

FDA Enforcement
Class I ·Terminated·CareFusion 303, Inc.·August 26, 2015