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

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Wrist Blood Pressure Monitor Model BP4350

FDA 510(k)
FDA Class 2 ·Cardiovascular

Curved Broach Handle - Supine

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215074661·

K181166

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code CBK·December 2, 2022

MASTERGRAFT STRIP

FDA 510(k)
FDA Class 2 ·Orthopedic

ELECTRO INTERSTITIAL SCAN

FDA 510(k)
FDA Class 2 ·Neurology

V60 VENTILATOR

FDA Adverse Event
Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code MNT·October 17, 2014

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·July 28, 2011

EON

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·June 14, 2013

FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC PROTEIN, COLLAGEN SCAFFOLD WITH MET

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·August 11, 2020

FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·September 17, 2018

FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·January 22, 2020

DEKA SMARTXIDE² TRIO

FDA Adverse Event
Malfunction ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·October 31, 2023

8110 ALARIS SYRINGE PUMP

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·February 8, 2021

8110 ALARIS SYRINGE PUMP

FDA Adverse Event
Malfunction ·CAREFUSION SD·Product code FRN·January 19, 2021

Medtronic MiniMed(TM) Quick-set(TM) (MMT-394, 394T, 399, 399T, 387, 387T, 398, 398T, 397, 397T, 386, 386T, 396, 396T)

FDA Enforcement
Class II ·Ongoing·Medtronic Inc.·November 29, 2017