37 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.

VARIANT II TURBO LINK HEMOGLOBIN A1C PROGRAM/TESTING SYSTEM

FDA 510(k)
FDA Class 2 ·Hematology

NITREX

FDA UDI
Covidien LP·10821684009007·Guidewire

NITREX™

FDA UDI
EV3, INC·00763000185343·GW N140801 NITREX V04

NITREX

FDA UDI
Covidien LP·00821684058107·Guidewire

VELNEZ

FDA UDI
DATT MEDIPRODUCTS PRIVATE LIMITED·08904340410654·VELNEZ Nasal Pack 8 cm x 1 cm

VELNEZ

FDA UDI
DATT MEDIPRODUCTS PRIVATE LIMITED·08904340411415·VELNEZ Nasal Pack 8 cm x 1 cm

n/a

FDA UDI
Ortho Development Corporation·00822409070374·Snap-on Fem Augment Trial 8mm Distal Size 4

n/a

FDA UDI
Ortho Development Corporation·00822409067121·Stem Extension Trial Diameter 14x80mm

Specials

FDA UDI
Seaspine Orthopedics Corporation·10889981441296·Straight Rake Curette with Teeth, Curved

INTRA-AORTIC BALLOON (IAB)

FDA 510(k)
FDA Class 2 ·Cardiovascular

PUMA MODEL VERSION 1.0

FDA 510(k)
FDA Class 2 ·Radiology

NITREX GUIDEWIRE/N140801

FDA Adverse Event
Injury ·EV3 PERIPHERAL VASCULAR DIVISION·Product code DQX·July 15, 2008

CLAREON IOL WITH THE AUTONOME DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·October 29, 2025

MAXZERO

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FPA·March 17, 2026

ACRYSOF IQ NATURAL SINGLEPIECE IOL

FDA Adverse Event
Malfunction ·ALCON RESEARCH, LLC - HUNTINGTON·Product code HQL·August 19, 2025

ACRYSOF IQ SINGLEPIECE IOL WITH ULTRASERT DELIVERY SYSTEM

FDA Adverse Event
Malfunction ·ALCON RESEARCH, LLC - HUNTINGTON·Product code HQL·April 20, 2026

CLAREON ASPHERIC UV ABSORBING IOL WITH AUTONOME DELIVERY SYSTEM

FDA Adverse Event
Injury ·ALCON LABORATORIES IRELAND LTD.·Product code HQL·October 31, 2025

GUARDIAN REAL-TIME MONITIOR

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code MDS·October 3, 2014

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Death ·BAXTER HEALTHCARE·Product code KDJ·May 31, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·May 31, 2011