10 results · 21ms · 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.

ARGYLE CONNECT TUBE-CON & NON

FDA 510(k)
FDA Class 2 ·General Hospital

ACUMED

FDA UDI
Acumed LLC·10806378105159·Small Frag 2-Level Case Base

VACUETTE WITH PPACK

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

TWISTCUT ENDOSORB SCREWS

FDA 510(k)
FDA Class 2 ·Orthopedic

PLUM 1.6 W/DATAPORT

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·February 21, 2014

FREESTYLE FLASH

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 1, 2007

UNKNOWN DEPUY SROM HIP LINER

FDA Adverse Event
Injury ·DEPUY RAYNHAM·Product code JDI·October 24, 2012

EVOLUT FX PLUS VALVE

FDA Adverse Event
Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 3, 2025

ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

FDA Enforcement
Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022

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