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

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NEODENT IMPLANT SYSTEM, TITAMAX TI EX ACQUA AND TI DRIVE ACQUA, TITAMAX SMART EX ACQUA AND DRIVE SMART ACQUA, TITAMAX CM

FDA 510(k)
FDA Class 2 ·Dental

ELATION® MB

FDA UDI
DENTSPLY SIRONA ORTHODONTICS INC.·D807K133552621·ELATION® MB Base Rx 022 UL/5-5 CS-BC HK

K133532

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·February 2, 2021

ENLIGHTN RENAL GUIDE CATHETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

REPROCESSED SURGICAL SCISSORS AND GRASPERS

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

M.U.S.T. PEDICLE SCREW 7X45

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MNI·January 20, 2017

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 29, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 8, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 11, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 26, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·March 5, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 19, 2026

MECHANICAL (MANUAL) WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code IOR·May 29, 2013

OCTRODE PERCUTANEOUS TRIAL LEAD

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 16, 2011

HIRES 90K

FDA Adverse Event
Malfunction ·ADVANCED BIONICS LLC·Product code MCM·August 20, 2008

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·May 18, 2026

CARDIOHELP

FDA Adverse Event
Malfunction ·MAQUET CARDIOPULMONARY GMBH·Product code DTQ·April 7, 2026

FLEXOR RADIAL ACCESS SET

FDA Adverse Event
Injury ·COOK, INC.·Product code DYB·April 13, 2015

PEDICLE SCREW 03.50.030 PEDICLE SCREW 7X40

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code KWP·February 3, 2020