646 results · 23ms · Sources: EU EUDAMED, US FDA

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TheraBase, TheraBase Ca

FDA 510(k)
FDA Class 2 ·Dental

Echo® Bi-Metric® Hip System

FDA UDI
Biomet Orthopedics, LLC·00887868260384·

Bernafon

FDA UDI
Bernafon AG·05711584086810·ZR3, KIT 312 NFM 75 L BE ZERENA 3

ECHO BI-METRIC HIP SYSTEM

FDA UDI
Biomet Orthopedics, LLC·00880304463066·

OsteoMed

FDA UDI
OSTEOMED LLC·00845694019040·2.0mm x 7mm Cannulated Lag Screw

CETRA

FDA UDI
Orthofix US LLC·18257200137435·CETRA - 2.0 SCREW CADDY, SEMI-CONSTRAINED SCREWS

OsteoMed

FDA UDI
OSTEOMED LLC·00845694070065·Cannulated 2.0 x 7mm Lag Screw Sterile Qty 5

CARTO 3 EP NAVIGATION SYSTEM, VERSION 2.2

FDA 510(k)
FDA Class 2 ·Cardiovascular

PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,

FDA 510(k)
FDA Class 2 ·Anesthesiology

ACRYSOF TORIC

FDA Adverse Event
Other ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·May 11, 2007

ACRYSOF

FDA Adverse Event
Injury ·ALCON LABORATORIES, INC/HUNTINGTON·Product code HQL·December 19, 2007

INRATIO

FDA Adverse Event
Malfunction ·HEMOSENSE, INC.·Product code JPA·January 31, 2007

ENDO GIA ROTICULATOR 60-3. 5 SULU

FDA Adverse Event
Injury ·NORTH HAVEN - USS·Product code GAG·February 1, 2007

SYNCHROMED EL

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·May 31, 2007

ACRYSOF

FDA Adverse Event
Injury ·ALCON LABORATORIES, INC. / HUNTINGTON·Product code HQL·March 21, 2007

PINN MAR +4NEUT 32IDX54OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 6, 2008

UNK ZIMMER HIP

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LZO·June 20, 2013

ADVANIX¿ BILIARY STENT WITH NAVIFLEX¿ RX DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SPENCER·Product code FGE·August 4, 2011

SYNTHETIC SLING MESH

FDA Adverse Event
Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·April 18, 2007

6.5MM TWINFIX AB SUTURE ANCHOR W/NEEDLES

FDA Adverse Event
Malfunction ·SMITH & NEPHEW INC., ENDOSCOPY DIV.·Product code MBI·January 23, 2008