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

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VAPOR-CLEAR, MODEL 100

FDA 510(k)
FDA Class 2 ·Anesthesiology

DELTA

FDA UDI
Stryker Leibinger GmbH & Co. KG·07613252598183·S-DRILLING TAP, HEX, FOR 5/6mm SCREW

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450237748·

MODIFICATION TO THERMAL ANGEL

FDA 510(k)
FDA Class 2 ·Hematology

PHACOFRAGMENTATION SYSTEM MEGATRON

FDA 510(k)
FDA Class 2 ·Ophthalmic

LINEAR ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 18, 2023

ANGIOJET ULTRA 5000A

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019

ANGIOJET ULTRA 5000A

FDA Adverse Event
Death ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019

ANGIOJET ULTRA 5000A

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORPORATION·Product code MCX·May 23, 2019

UNKNOWN LINER

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·August 7, 2017

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·May 3, 2013

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·September 16, 2014

HOMECHOICE PRO

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - TAMPA·Product code FKX·May 18, 2011

MANTIS REDUX BLOCKER

FDA Adverse Event
Malfunction ·STRYKER SPINE-US·Product code NKB·November 27, 2019

TIBIAL NAIL-ADVANCED / 9 345 / STERILE

FDA Adverse Event
Injury ·SYNTHES GMBH·Product code HWC·February 27, 2023

TIBIAL NAIL ADVANCED Ø10 L315

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code JDS·April 7, 2023

5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 34MM

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code KTT·June 23, 2023

5.0MM TI LOCKING HEAD SCREW SELF-TAPPING 38MM

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code KTT·June 23, 2023