49 results · 23ms · 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.

Vscan Air

FDA 510(k)
FDA Class 2 ·Radiology

OsteoMed

FDA UDI
OSTEOMED LLC·00845694041393·3.5mm Over Drill, Quick Release

Conventional Lead Apron .5mm Xtra Large 25 X 40

FDA UDI
Flow X Ray Corporation·00843696123697·Conventional Lead Apron .5mm Xtra Large 25 X 40...

SprintRay Standard Denture Teeth - A3

FDA UDI
Sprintray, Inc.·00850039704376·SprintRay Standard Denture Teeth is a light-cur...

Corneal Trephine

FDA UDI
KATENA PRODUCTS, INC.·00841668112489·BARRON VACUUM TREPHINE 7.25MM

VICEROY Spinal System

FDA UDI
EOS BIOTEK,INC.·88000163009016·

Viceroy

FDA UDI
DIOMEDICAL CO.,LTD.·08800039826242·Rod Pre-Bent 6.0 x 35mm

OsteoMed

FDA UDI
OSTEOMED LLC·00845694073462·FPS 3.5mm Over Drill, Quick Release Sterile Qty 2

SLEEK OTW PTA CATHETERS

FDA 510(k)
FDA Class 2 ·Cardiovascular

OSTEOMEDICS RESORBABLE SMALL FIXATION SYSTEM, OSTEOSORB

FDA 510(k)
FDA Class 2 ·Dental

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FPA·May 26, 2021

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·June 17, 2021

UNK_SMART TOUCH BIDIRECTIONAL

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code LPB·September 25, 2022

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code LHI·March 8, 2021

GROSHONG NXT CLEARVUE 4F SINGLE-LUMEN PICC BASIC TRAY (WITH MICROINTRODUCER)

FDA Adverse Event
Malfunction ·BARD ACCESS SYSTEMS·Product code LJS·July 30, 2020

SMARTSITE 20MM VENTED VIAL ACCESS DEVICE

FDA Adverse Event
Malfunction ·Product code FPA·June 10, 2021

BD INTIMA-II CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·BD (SUZHOU)·Product code FOZ·October 1, 2020

UNKNOWN ENDO GIA SULU

FDA Adverse Event
Injury ·COVIDIEN LP LLC NORTH HAVEN·Product code GDW·November 4, 2020

PREMICATH

FDA Adverse Event
Injury ·VYGON GMBH·Product code LJS·April 13, 2021

UNICEL DXC 600 SYNCHRON CLINICAL SYSTEM

FDA Adverse Event
Injury ·BECKMAN COULTER, INC.·Product code JGS·August 5, 2011