10 results · 26ms · Sources: EU EUDAMED, US FDA

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DEPUY DELTA XTEND REVERSE SHOULDER HIGH MOBILITY CUP

FDA 510(k)
FDA Class 2 ·Orthopedic

TRIDENT HEMISPHERICAL ACETABULAR SHELLS

FDA 510(k)
FDA Class 2 ·Orthopedic

RITA MODEL 2500 ELECTROSURGICAL RF GENERATOR

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·April 23, 2013

ZEPHYR XL DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code LWP·September 9, 2014

EON IMPLANTABLE PULSE GENERATOR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·April 13, 2011

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code DZI·October 6, 2020

NSK

FDA Adverse Event
Injury ·NAKANISHI INC.·Product code DZI·July 15, 2025

NSK

FDA Adverse Event
Malfunction ·NAKANISHI INC.·Product code ELC·September 9, 2016

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