28 results · 23ms · Sources: EU EUDAMED, US FDA

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GENERIC BLOOD GLUCOSE TEST STRIP

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Henry Schein

FDA UDI
HENRY SCHEIN, INC.·00304040062418·Endoflex Reamers 25 mm

CUSTOM PROCEDURE KIT

FDA UDI
MEDIVATORS INC.·40677964009868·The ENDO CARRY-ON Procedure Kit contains all of...

Implant Prosthetics

FDA UDI
Preat Corporation·00842092102213·Branemark®-compatible RP 30° Multi-Unit Abutmen...

Epredia

FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693214636·Cassettes are designed to contain incised tissu...

artVeneer life

FDA UDI
Merz Dental GmbH·D7092001092·artVeneer life lower anteriors, UBS, A3

CD61 APC

Basic UDI-DI
EU IVDD · Eu Ivd General ·Shenzhen Wellgrow Biotech Co., Ltd.·1 device

E3 MICROPROB SERIES OF LASERS AND ACCESSORIES

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

WAKO LIPASE CALIBRATOR

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

SYNCARDIA FREEDOM ONBOARD BATTERY

FDA Adverse Event
Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 19, 2022

SYNCARDIA FREEDOM ONBOARD BATTERY

FDA Adverse Event
Malfunction ·SYNCARDIA SYSTEMS, LLC·Product code LOZ·October 21, 2022

STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

IMPAX CV REPORTING

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·February 26, 2013

HOMECHOICE

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·February 24, 2011

NOVASURE IMPEDANCE CONTROLLED EA SYSTEM

FDA Adverse Event
Injury ·CYTYC SURGICAL PRODUCTS·Product code MNB·February 22, 2008

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

RIBFIX BLU SYSTEM CROSS DRIVE BLADE, LONG

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·May 23, 2019

COBALT HV BONE CEMENT 40G

FDA Adverse Event
Injury ·BIOMET ORTHOPEDICS·Product code LOD·February 9, 2012

SYRINGE BOIN TUBE 10ML 21G 1-1/4IN

FDA Adverse Event
Malfunction ·BECTON DICKINSON·Product code FMF·October 13, 2020