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

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Easy-Load Lens Delivery System

FDA 510(k)
FDA Class 1 ·Ophthalmic

Cohere

FDA UDI
Nuvasive, Inc.·00887517014047·COHERE TLIF-O Trial, 16x10mm 12°

OSS™ Orthopedic Salvage System

FDA UDI
Biomet Orthopedics, LLC·05019279057580·

ORTHOPEDIC SALVAGE SYSTEM (OSS)

FDA UDI
Biomet Orthopedics, LLC·00880304250772·

TALOS® IBF

FDA UDI
MEDITECH SPINE, LLC·B167311610120·

TALOS® HA PEEK IBF

FDA UDI
MEDITECH SPINE, LLC·B167321610120·

10PC - UP - 380-54620 - Locamotive

FDA UDI
Certified Safety Manufacturing, Inc.·00766588110127·10PC - UP - 380-54620 - Locamotive

V-TRUST HANDHELD PULSE OXIMETER MODEL: TD-8201

FDA 510(k)
FDA Class 2 ·Cardiovascular

AXSOS PLUS LOCKING PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

MiniSPC Button

FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071150358·16F x 1.0cm MiniSPC Low Profile Suprapubic Cath...

MiniSPC Button

FDA UDI
APPLIED MEDICAL TECHNOLOGY, INC.·00842071147730·16F x 1.0cm MiniSPC Low Profile Suprapubic Cath...

ACCELERATOR A3600

FDA Adverse Event
Malfunction ·INPECO SA·Product code JQP·December 20, 2024

CAPSUREFIX NOVUS

FDA Adverse Event
Malfunction ·MPRI·Product code DTB·October 10, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

COULTER LH 750 HEMATOLOGY ANALYZER

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code GKZ·June 17, 2011

OSS INTERLOK IM STEM W/SCREW

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 23, 2018

CPS SM SPDL WITH PINS 600LBF

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDC·July 31, 2019

OSS RS AXLE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·July 31, 2019

OSS TIBIAL POLY BEARING 12MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 31, 2019

OSS MOD TIB BASEPLATE 79MM

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·July 31, 2019