10 results · 27ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

TITANIUM MESH

FDA 510(k)
FDA Class 2 ·Neurology

Brigade

FDA UDI
Nuvasive, Inc.·00887517962973·Brigade Lateral Trial, 10x34x32mm 30°

CARE PROVIDER STATION ADDITION OF WEIGHT SCALE

FDA 510(k)
FDA Class 2 ·Cardiovascular

VESISCAN

FDA 510(k)
FDA Class 2 ·Radiology

STEALTHSTATION¿ S8 SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 8, 2025

SWIFTSET TOPICAL SKIN ADHESIVE

FDA Adverse Event
Malfunction ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code MPN·July 9, 2015

VASO VIEW HEMOPRO

FDA Adverse Event
Injury ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·January 3, 2013

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 26, 2007

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·April 14, 2015

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