35 results · 24ms · Sources: EU EUDAMED, US FDA

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DSI PINS AND WIRES

FDA 510(k)
FDA Class 2 ·Orthopedic

Sprint®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70606541·Sprint II Brackets Roth .022" 400 Brackets

VBMAX

FDA 510(k)
FDA Class 2 ·Anesthesiology

AT HOME DRUG TEST, MODEL 9078 T

FDA 510(k)
FDA Unclassified ·Unknown

TESS HUM INSERT TH 6 DIA36 S1

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·March 7, 2017

TESS HUMERAL INSERT TH 8 DIA36 S0

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

TESS HUMERAL REVERSED INLAY 036 S1 12MM

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 9, 2017

TESS HUMERAL INSERT TH 6 DIA36 S0

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 15, 2017

CUSTOM REVERSE HUMERAL LINER

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 27, 2017

STELO GLUCOSE BIOSENSOR SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code SAF·March 13, 2025

TESS GLEN BASEPLATE S0

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 25, 2016

TESS HUMERAL REVERSE COROLLA S0

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·November 18, 2016

UNKNOWN TESS GLENOID COMPONENT

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·July 7, 2017

TESS HUM INSERT TH 6 DIA36 S0

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·May 10, 2017

UNKNOWN TESS HUMERAL INSERT

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·June 1, 2017

840 VENTILATOR

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY NELLCO·Product code CBK·April 5, 2013

MEDTRONIC

FDA Adverse Event
Injury ·MEDTRONIC INC.·Product code DTE·June 10, 2008

LIGASURE IMPACT

FDA Adverse Event
Malfunction ·COVIDIEN LP (VALLEYLAB)·Product code GEI·April 8, 2011

TESS HUMERAL INSERT TH 8 DIA36 S0

FDA Adverse Event
Malfunction ·BIOMET FRANCE S.A.R.L.·Product code KWS·February 17, 2017

TESS HUMERAL INSERT TH 6 DIA36 S0

FDA Adverse Event
Injury ·BIOMET FRANCE S.A.R.L.·Product code KWS·January 25, 2017