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

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MULTIFUNCTIONAL LINEAR PEN

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

Bur PM2-MIS D150 diam Ø3.0 St

FDA UDI
Bien-Air Surgery SA·17630055506297·

Ni-Ti - Archwire

FDA UDI
ORMCO CORPORATION·00889989027068·NI-TI BROAD ARCH UPSML 0175 0175 PK10

OsteoMed

FDA UDI
OSTEOMED LLC·00845694002110·Mini, Locking Strut Plate, Curved, 2x4 Hole

ENDO SMARTCAP (100501)

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869679619·MOSS MIS XT Rod Inserter

NA

FDA UDI
Biedermann Motech GmbH & Co. KG·04250869608206·TELIX K Inserter Cage/Trial

General Instrument

FDA UDI
ALPHATEC SPINE, INC.·00840180509760·Curved Thoracic Probe, Ball Handle

MOBIVISION

FDA 510(k)
FDA Class 2 ·Radiology

ELECTROSURGICAL GENERATOR, MODEL S1

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

1818910-2019-100501

FDA Adverse Event
Injury ·August 8, 2019

ALEUTIAN SPACER, MODEL K2-07-1004-01, K2-07-1005-01

FDA 510(k)
FDA Class 2 ·Orthopedic

FREESTYLE LIBRE 3 PLUS

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC·Product code QBJ·April 30, 2026

A100501S

Basic UDI-DI
EU IVDD · Eu Ivd General ·Hangzhou Cybereagen Biotech Co., Ltd.·1 device

K1025-01-EDT

Basic UDI-DI
EU MDR · Eu Md Class 2a ·6 devices

PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·May 8, 2013

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DTQ·May 13, 2011

GALAXY G3 MINI 2MM X 4CM

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SARL·Product code KRD·October 26, 2020

GALAXY G3 2.5MM X 5CM

FDA Adverse Event
Death ·MEDOS INTERNATIONAL SARL·Product code KRD·October 14, 2020