20 results · 46ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

Beta Mini

FDA UDI
B& L Biotech, inc.·08800019101154·

Beta Mini

FDA UDI
B& L Biotech, inc.·08800019101659·

Beta Mini(W)

FDA UDI
B& L Biotech, inc.·08800019101666·

Beta Mini(P)

FDA UDI
B& L Biotech, inc.·08800019101178·

Beta Mini(P)

FDA UDI
B& L Biotech, inc.·08800019101673·

Beta Mini(W)

FDA UDI
B& L Biotech, inc.·08800019101161·

DUOHEX CH CANNULATED HAMMERTOE SYSTEM

FDA Adverse Event
Malfunction ·NEXTREMITY SOLUTIONS, INC.·Product code HWC·April 26, 2021

DUOHEX CH CANNULATED HAMMERTOE SYSTEM

FDA Adverse Event
Malfunction ·NEXTREMITY SOLUTIONS, INC.·Product code HWC·April 26, 2021

BD PYXIS ANESTHESIA STATION ES

FDA Adverse Event
Injury ·CAREFUSION 303, INC.·Product code BRY·October 17, 2022

MEDTRONIC 780G PUMP AND RELATED CGM

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OZP·February 4, 2026

MINICAP TRANSFER SET

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·August 7, 2013

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·January 29, 2022

FILLER, CALCIUM SULFATE PREFORMED PELLETS

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code MQV·May 18, 2018

BODYGUARDIAN MINI EL

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CARDIAC DIAGNOSTIC TECHNOLOGIES, INC.·Product code DSI·December 1, 2025

AIA-2000

FDA Adverse Event
Malfunction ·TOSOH HI-TEC, INC.·Product code KHO·February 11, 2026

WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NGV·March 25, 2024

ESSURE

FDA Adverse Event
Injury ·BAYER PHARMA AG·Product code HHS·March 21, 2018

SFTWR MMT-6122 FOTA IOS OUS/US

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OUG·September 8, 2023

TAXUS EXPRESS2 PACLITAXEL-ELUTING CORONARY STENT

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·May 26, 2006

EMERGE

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code LOX·March 18, 2021