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