77 results · 31ms · Sources: EU EUDAMED, US FDA

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NUVASIVE VUEPOINT OCT SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

K091319

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·January 9, 2026

NONIN MODEL 2120 PULSE OXIMETER AND NONINVASIVE BLOOD PRESSURE (NIBP) MONITOR

FDA 510(k)
FDA Class 2 ·Cardiovascular

NUVASIVE MASH

FDA 510(k)
FDA Class 2 ·Orthopedic

REMSTAR AUTO A-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·January 12, 2026

UNKNOWN

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

UNKNOWN

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

UNKNOWN

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·December 16, 2019

REMSTAR AUTO A-FLEX, SYS ONE, 60 SRS, FR

FDA Adverse Event
Injury ·RESPIRONICS, INC·Product code BZD·August 5, 2021

EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT-FULLY COVERED

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·March 25, 2015

REMSTAR PRO C-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·December 31, 2025

REMSTAR

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·October 22, 2024

BIPAP PRO BIFLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·March 5, 2026

REMSTAR

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·October 28, 2024

DREAMSTATION AUTO CPAP

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·April 10, 2025

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·January 7, 2026

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 6, 2013

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code ITI·September 16, 2014

PARADYM

FDA Adverse Event
Malfunction ·SORIN CRM S.R.L.·Product code MRM·April 15, 2011

REMSTAR PLUS C-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·July 17, 2024