16 results · 21ms · 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.

VEIN-GOGH INSTRUMENT

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

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04047872673204·LEVAMED STABILI-TRI ANKLE SUP BLU R IV

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950017485·RETRACTOR SURGICAL CURVED DOWN 14X70MM 8-1/2" 21CM

SOL-M™ Hypodermic Needle

FDA UDI
Sol-Millennium Medical, Inc.·00818392015232·Sterile hypodermic needles intended to inject f...

Pusher/Extender

FDA UDI
ELLIQUENCE, LLC·00846338001797·

TRANS1 AXIALIF PLUS

FDA 510(k)
FDA Class 2 ·Orthopedic

CONTOUR MENISCUS ARROW, MODELS 541110, 541113, AND 541116

FDA 510(k)
FDA Class 2 ·Orthopedic

600 ML TRANSFER BAG

FDA Adverse Event
Malfunction ·CHARTER MEDICAL·Product code KSR·July 15, 2007

PEN NDL 31GA 8MM 14BAG 700CAS JP

FDA Adverse Event
Malfunction ·BECTON DICKINSON AND CO.·Product code FMI·September 29, 2020

OSS POLY TIBIAL BUSHING

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code JDI·May 14, 2013

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·September 23, 2014

LIGASURE ATLAS HANDSWITCHING 37CM

FDA Adverse Event
Injury ·COVIDIEN LLC (SHANGHAI)·Product code GEI·May 25, 2011

MEDTRONIC ICD

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·May 29, 2020

GMK REVISION TOTAL KNEE SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·March 31, 2026

INLIVEN CRT-P, Model Numbers: a) V284 b) V285 c) W274 d) W275 (added 7/15/2021)

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·July 21, 2021

Model Number L131, ESSENTIO DR EL MRI Pacemaker

FDA Enforcement
Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025