20 results · 22ms · Sources: EU EUDAMED, US FDA

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H/S CATHETER SET 5 FRENCH, MODEL 61-5005F, H/S CATHETER SET 7 FRENCH, MODEL 61-5007F

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

DOUBLE SPRINGERS NONOXNOL 9 CONDOM

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

XLTEK EVOKED POTENTIAL HEADBOX, MODEL EP-8

FDA 510(k)
FDA Class 2 ·Neurology

PRECISION SPECTRA

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 24, 2021

DA VINCI SI SURGICAL SYSTEM

FDA Adverse Event
Death ·INTUITIVE SURGICAL,INC.·Product code NAY·May 3, 2013

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 16, 2014

3F X 60CM SINGLE VASCU-PICC

FDA Adverse Event
Malfunction ·MEDCOMP·Product code LJS·April 15, 2011

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

ROD Ø5.5 SOFT CURV L70 TI

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 5, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

PEDICSCR MATRIX 5.5 POLYAXIAL Ø6 PREASSM

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

ROD Ø5.5 SOFT CURV L70 TI

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code NKB·November 6, 2013

NEUROVENT-P (092946-003); NEUROVENT (092956-003); NEUROVENT-IFD-R (095317-003); NEUROVENT-IFD-S (091678-003); NEUROVENT-P-TEMP (094268-003); NEUROVENT-TEMP (094278-003); NEUROVENT-TEMP-IFD-R (095327-003); NEUROVENT-TEMP-IFD-S (094288-003); NEUROVENT-PTO (095008-003); NEUROVENT-PTO 2L (095108-003); NEUROVENT-PX (091580-003); BOLT-DRILL KIT CH5 (091888-003); BOLT-DRILL KIT CH9 (091898-003); BOLT-DRILL KIT PTO (092380-003); BOLT-DRILL KIT VP 16 (092969-003); BOLT KIT CH5 (091868-003); BOL

FDA 510(k)
FDA Class 2 ·Neurology

Stryker MA204 Bed Model (FL25E) Beds are intended for medical purposes in both general patient care as well as critical care environments. Each uses built-in electric motors and controls which can be operated by the patient, or caregiver, to adjust the height and/or surface contour of the bed.The devices listed above also include movable and latchable side rails which can be lowered or raised to help prevent patient fall and subsequent injury. The Beds include an optional Scale (Models: FL20E, FL25E, FL28C, FL28EX) as well as an optional Bed Exit (1 Zone) or Chaperone

FDA Enforcement
Class II ·Terminated·Stryker Medical Division of Stryker Corporation·July 4, 2012