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

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TissueStat

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

ELMED

FDA UDI
ELMED INCORPORATED·00842180161108·PRISM CERVICAL CURETTE 10" ANGLED 2-0, GOLD

SEVIIN FRACTURE SHOULDER

FDA 510(k)
FDA Class 2 ·Orthopedic

JOWIRE ASAHI PTCA CATHETER GUIDE WIRES, MODELS AG145300,141300,142300,132200,14M350,14M345,14M360,143390,141002

FDA 510(k)
FDA Class 2 ·Cardiovascular

TENDRIL ST

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·November 6, 2014

INRATIO2

FDA Adverse Event
Malfunction ·ALERE SAN DIEGO INC·Product code GJS·July 25, 2011

NAVIGATORTM HD

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SPENCER·Product code KOD·July 17, 2013

UNSPECIFIED BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE TUBES

FDA Adverse Event
Malfunction ·BECTON DICKINSON & CO (FRANKLIN LAKES)·Product code JKA·October 15, 2025

BD VACUTAINER® SODIUM FLUORIDE/POTASSIUM OXALATE 5MG/4MG

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·May 23, 2024

CARTO 3

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·September 16, 2024

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·May 21, 2024

CARTO 3

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·October 28, 2025

CARTO® 3 SYSTEM

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·April 17, 2024

CARTO 3

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER INC·Product code DQK·October 15, 2025

Revogene, Catalog no. 610210. IVD test instrument

FDA Enforcement
Class II ·Ongoing·Meridian Bioscience Inc·August 3, 2022

UNIVERSAL Modular Electric/Battery Handpiece for surgery The electric handpiece is packaged within a foam bag inside of a padded-foam corrugate box. An operating manual is packed with the handpiece between the top foam pad and box lid. A product label is applied to the lid of the box. Product Usage: Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.

FDA Enforcement
Class II ·Terminated·Zimmer Surgical Inc·November 12, 2014