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