13 results · 23ms · Sources: EU EUDAMED, US FDA

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CAPLESS PEDICLE SCREW SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 3, 2020

EXCISOR BIOPTOME, MODEL 01-0004

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

INTRODUCER WITH DISTAL RADIOPAQUE MARKER BAND, MODEL OR-4926XX

FDA 510(k)
FDA Class 2 ·Cardiovascular

CONTOUR THREAD OR CONTOUR THREADS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES (DBA ANGIOTECH)·Product code GAW·April 3, 2008

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code LXH·March 31, 2017

2.7MM TI VA LCKNG SCR SLF-TPNGWITH T8 STARDRIVE RECESS 14MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·April 11, 2013

CONTAK RENEWAL

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 13, 2011

ACCU-CHEK ULTRAFLEX INFUSION SET

FDA Adverse Event
Malfunction ·DISETRONIC MEDICAL SYSTEMS·Product code FPA·May 27, 2008

BD INTIMA-II Y 24GAX0.75IN PRN EC SLM NPVC

FDA Adverse Event
Malfunction ·BD SUZHOU (MDS)·Product code FOZ·April 3, 2024

CD HORIZON® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code NKB·December 29, 2024

BD INTIMA-II¿ CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·October 23, 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