21 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
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