21 results · 21ms · Sources: EU EUDAMED, US FDA

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ZIRCONIA CERAMIC FEMORAL HEADS WITH FOUNDATION FORGED, TEXTURED AND POROUS STEMS, THE ENCORE VITALITY STEMS AND SL AND

FDA 510(k)
FDA Class 2 ·Orthopedic

Acrometrix HBV Mid Control

FDA UDI
Microgenics Corporation·00884883006508·

EDP-10 INVIVO Detector

FDA UDI
IBA Dosimetry GmbH·EIBA9650020·EDP-10 3G-pSi Semiconductor detector, 2m cable

N/A

FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024368859·Bed Frame Adaptor Assembly

A-BEC 18

FDA 510(k)

SINGLE USE MANUAL RESUSCITATORS

FDA 510(k)
FDA Class 2 ·Anesthesiology

ZMR®

FDA UDI
Zimmer, Inc.·00889024158603·

ZMR®

FDA UDI
Zimmer, Inc.·00889024158610·

ZMR®

FDA UDI
Zimmer, Inc.·00889024158597·

UNK BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·June 23, 2025

BONE SCREW SELF-TAPPING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 28, 2025

BONE SCREW SELF-TAPPING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 28, 2025

BONE SCREW SELF-TAPPING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 28, 2025

ECHO BI-METRIC HIP SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 28, 2025

G7 OSSEOTI ACETABULAR SHELL

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 28, 2025

VIRTUOSO VR

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LWS·February 15, 2013

PRECISION TEST STRIPS

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 20, 2011

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 29, 2014

Zimmer Patient Helper Bed Frame Adapter Assembly The bed frame adapter assembly is intended to be used by qualified medical professionals to adapt a patient helper to a hospital bed. The patient helper is used to aid and assist the patient's mobility within a hospital bed and during bed ingress and egress.

FDA Enforcement
Class II ·Terminated·Zimmer, Inc.·June 26, 2013

G7 DUAL MOBILITY ACETABULAR SYSTEM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code LPH·March 28, 2025