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

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STELKAST PROVEN KNEE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Procure

FDA UDI
Twin Med, LLC·10840330700563·Oxygen Tubing Swivel Connector

Oxygen Tubing

FDA UDI
WESTMED, INC.·00709078014086·Oxygen Tubing Swivel Connector (TwinMed)

Implant Prosthetics

FDA UDI
Preat Corporation·00842092102756·Astra®-compatible Lilac 4.5/5.0mm 17° Multi-Uni...

Implant Prosthetics

FDA UDI
Preat Corporation·00842092131268·Astra®-compatible Lilac 4.5/5.0mm 17° Multi-Uni...

WALLSTENT ENTERNAL PROSTHESIS

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

GERATHERM BABYWATCH TEMPERATURE MONITOR

FDA 510(k)
FDA Class 2 ·General Hospital

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO-SURGERY, INC.(CINCINNATI)·Product code LFL·June 2, 2006

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

ULTRACISION SURG DEV, CURVED SHEARS, OPEN

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code LFL·June 7, 2006

ULTRACISION SURG DEV, CURVED SHEARS, ENDO

FDA Adverse Event
Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GEI·June 19, 2006

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·March 13, 2013

HUDSON DUAL LIMB HEATED NEONATAL CIRCUIT

FDA Adverse Event
Malfunction ·TELEFLEX MEDICAL·Product code BTT·January 25, 2011

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·February 22, 2008

APTIMA SARS-COV-2 ASSAY

FDA Adverse Event
Malfunction ·HOLOGIC INCORPORATED·Product code QJR·May 5, 2022