711 results
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29ms
·
Sources: EU EUDAMED, US FDA
LED Curing Light
FDA 510(k)
FDA Class 2
·Dental
ECHO BI-METRIC HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304463318·
Echo® Bi-Metric® Hip System
FDA UDI
Biomet Orthopedics, LLC·00887868260407·
Bernafon
FDA UDI
Bernafon AG·05711584086834·ZR3, KIT 312 NFM 85 L BE ZERENA 3
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776199838·LLETZ GRAVES SPEC LG wEvac
OsteoMed
FDA UDI
OSTEOMED LLC·00845694019057·2.0mm x 9mm Cannulated Lag Screw
OsteoMed
FDA UDI
OSTEOMED LLC·00845694070102·Cannulated 2.0 x 9mm Lag Screw Sterile Qty 5
AIDA VI.8 DIAGNOSTIC ULTRASOUND GM-72P00A, L13-5V1 TRANSDUCER
FDA 510(k)
FDA Class 2
·Radiology
MODIFICATION TO: LEVEEN SUPERSLIM NEEDLE ELECTRODES, MODELS M001262260, M001262270, M001262280, M001262290
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ARSENAL PETITE LAPIDUS PLATE, R
FDA Adverse Event
Injury
·TRILLIANT SURGICAL·Product code HRS·April 3, 2020
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD·Product code MCM·September 2, 2009
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·February 11, 2009
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH. LTD.·Product code HQL·July 2, 2009
ACRYSOF TORIC
FDA Adverse Event
Injury
·ALCON RESEARCH LTD / HUNTINGTON·Product code MJP·November 11, 2009
OLSEN
FDA Adverse Event
Other
·OLSEN MEDICAL·Product code GEI·March 12, 2009
S-ROM M HEAD 36MM +0
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code JDI·October 6, 2008
NEXGEN STEMMED TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER·Product code JWH·June 20, 2013
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 4, 2011
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·May 20, 2009
TIMAX
FDA Adverse Event
Malfunction
·NSK TOCHIGI-KEN (JAPAN)·Product code EGS·October 15, 2009