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

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MODIFIED MERCI RETRIEVER, MODEL 90092

FDA 510(k)
FDA Class 2 ·Cardiovascular

Mini-Sprint®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70610591·Mini Sprint-Brackets 5-5 McLaugh/Benn/Trev. .02...

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172973202·

INFARED EAR THERMOMETER, MODEL TH8 SERIES

FDA 510(k)
FDA Class 2 ·General Hospital

NORMOCARB STERILE BICARBONATE RENAL DIALYSIS

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

STYLE 68 SALINE FILLED BREAST IMPLANT

FDA Adverse Event
Injury ·ALLERGAN (COSTA RICA)·Product code FWM·July 28, 2020

AEQUALIS REVERSED CEMENTLESS METAPHYSIS HA D.36MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·May 30, 2023

FENESTRATED BIPOLAR FORCEPSINSTRUMENT

FDA Adverse Event
Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 16, 2013

STERIS ST BACK 902, SHOULDER CHAIR

FDA Adverse Event
Other ·ALLEN MEDICAL SYSTEMS·Product code FWZ·February 22, 2011

VERSYS HIP SYSTEM FEMORAL STEM FIBER METAL TAPER COLLARLESS

FDA Adverse Event
Malfunction ·ZIMMER, INC.·Product code KWY·June 13, 2008

AEQUALIS REVERSED GLENOSPHERE 10 DEGREES TILTED 36 MM X 25MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·April 25, 2022

AEQUALIS REVERSED CEMENTLESS METAPHYSIS HA D.36MM

FDA Adverse Event
Injury ·TORNIER S.A.S.·Product code KWS·April 20, 2023

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

CADD¿- Solis Ambulatory Infusion Pump, Model 2111 & 2112, Version 1.0, Version 2.0 and Version 3.0 & Model 2120, Version 1.0. Provide measured drug therapy to patients in hospital or outpatient settings.

FDA Enforcement
Class II ·Terminated·Smiths Medical ASD, Inc.·June 24, 2015