30 results · 22ms · Sources: EU EUDAMED, US FDA

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INTERFUSE L INTERVERTEBRAL BODY FUSION DEVICE

FDA 510(k)
FDA Class 2 ·Orthopedic

PIVOX™ Oblique Lateral Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169605084·SPACER 2131540 OLIF25 27MM 6 DEG 16X40

NC Screw-retained Abutment

FDA UDI
BIO CONCEPT Co., Ltd.·06947600303381·

ArgenIS

FDA UDI
ARGEN CORPORATION, THE·D818131540·MUA SB RC 4.5GH Ang30

OsteoMed

FDA UDI
OSTEOMED LLC·00845694046183·PrimaLIF LLIF PEEK Implant, 15mm X 22mm X 40mm,...

Freedom Pedicle Screw System

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215027049·

CREATION

FDA UDI
Gc Orthodontics America Inc.·D78813154000101·CREATION ROTH 018/U4&5 -7T 0A

IH 15° Anatomic Abutment

FDA UDI
SURCAM - MEDICAL DEVICES AND DEVELOPMENTS LTD·07290120484382·

APEX ELECTRIC HANDPIECE SYSTEM

FDA 510(k)
FDA Class 1 ·Dental

GRANITEC DUAL-CURE CORE BUILD-UP, N'DURANCE DIMER CORE

FDA 510(k)
FDA Class 2 ·Dental

BIM400 IMPLANT MAGNET

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·December 19, 2017

COCHLEAR BAHA ATTACT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·June 26, 2016

ATTRACT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 15, 2015

COCHLEAR BAHA ATTACT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016

BIM400 IMPLANT MAGNET

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 17, 2016

SP MAGNET 3

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·September 13, 2016

COCHLEAR BAHA ATTRACT SYSTEM

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·August 14, 2016

BIM400 IMPLANT MAGNET

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·October 8, 2025

SURESCAN

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·October 1, 2014

SONOSURG SCISSORS 5MM O.D., HF SERIES

FDA Adverse Event
Malfunction ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code LFL·May 15, 2013