29 results · 24ms · Sources: EU EUDAMED, US FDA

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WEGO-PDO Barbed Suture

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

Ophthalmic Cannula

FDA UDI
KATENA PRODUCTS, INC.·00841668113936·GIANNETTI "BIG SPURT" CANNULA 21GA

TRULINE REINFORCED VALVED INFUSION CATHETER

FDA 510(k)
FDA Class 2 ·General Hospital

PREFACE GUIDING SHEATH, MODELS 2-603M, 2-703M, 2-803M, 2-903M, 2-1003M, 2-1103M

FDA 510(k)
FDA Class 2 ·Cardiovascular

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·August 12, 2024

HOLDING SLEEVE-LONG FOR MATRIX

FDA Adverse Event
Malfunction ·SYNTHES MONUMENT·Product code LXH·September 18, 2014

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·November 13, 2018

VICRYL POLYGLACTIN 910 SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAM·November 13, 2018

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·November 13, 2018

ETHIBOND EXTRA & EXCEL POLYESTER SUTURE UNKNOWN

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAT·November 13, 2018

MERSILENE TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code KDC·November 13, 2018

MERSILENE TAPE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code KDC·November 13, 2018

WALLFLEX DUODENAL

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MUM·January 22, 2025

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 27, 2014

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·August 11, 2011

LEAD MODEL UNKNOWN

FDA Adverse Event
Malfunction ·CYBERONICS INC·Product code LYJ·July 2, 2013

INRATIO

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·January 21, 2011

BD PHASEAL¿ PROTECTOR P14

FDA Adverse Event
Malfunction ·BECTON DICKINSON, S.A.·Product code ONB·July 27, 2022

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·May 27, 2022

UNKNOWN SUTURE ANCHOR

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code KWS·October 15, 2014