19 results · 21ms · Sources: EU EUDAMED, US FDA

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DISPENSER, TECHNETIUM, CLINTICHEM

FDA 510(k)
FDA Class 2 ·Radiology

Aquasence

FDA UDI
Drive Devilbiss Healthcare·00754021216062·Bath SafetyBenches/Stools Product Description: ...

BOSS Instruments

FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515199286·Aufranc Cobra Retr, smooth pointy tip, 8 1/2"

The Orthodontic Store

FDA UDI
Young Innovations, Inc.·00843471184073·.022 U/L Std. Sngl Weld Sz#15

Aquasense

FDA UDI
Drive Devilbiss Healthcare·07540212160626·AQS Adj. Bath Stool, 2EA/CV

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055611·OMNIARCH® EURO 022 UL/5-5 CS HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055221·OMNIARCH® Base Rx 022 UL/5-5 CS-BC HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055621·OMNIARCH® EURO 022 UL/5-5 CS-BC HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055131·OMNIARCH® Base Rx 018 UL/5-5 CS HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055121·OMNIARCH® Base Rx 018 UL/5-5 CS-BC HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055281·OMNIARCH® CETLIN® 022 UL/5-5 CS HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055231·OMNIARCH® Base Rx 022 UL/5-5 CS HK

OMNIARCH®

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K77055301·OMNIARCH® BI-DIMENSIONAL® UL/5-5 CS HK

Sterile Nitrile Surgical Gloves, Powder-free

FDA 510(k)
FDA Class 1 ·General, Plastic Surgery

A-VIEW BASIC AND PLUS

FDA 510(k)
FDA Class 2 ·Radiology

FREESTYLE

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code NBW·June 19, 2007

VASOVIEW 6 PRO

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·January 21, 2014

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 3, 2012

Ocular Conformer, Sterile, Porex Surgical Inc., 15 Dart Road, Newnan, GA 30265. The device is intended to be used as a post eye surgery device to prevent closure or adhesion during the healing process.

FDA Recall
Terminated ·Porex Surgical, Inc.·Product code HQN·March 28, 2008