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

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BIOMEDICS (OCUFILCON D) SOFT (HYDROPHILIC) CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450460474·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450252178·

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450399149·

K091319

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

QUEST EXERCISE STRESS SYSTEM, MODEL CONFIGURATION 14

FDA 510(k)
FDA Class 2 ·Cardiovascular

MRI FASTSYSTEM RETRACTOR SYSTEM

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

REMSTAR AUTO A-FLEX

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

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

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

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

ACCENT DR RF

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·January 14, 2014

ACCUTORR V MONITOR

FDA Adverse Event
Malfunction ·MINDRAY DS USA, INC.·Product code DXN·April 30, 2013

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code MDS·May 5, 2011

REMSTAR PLUS C-FLEX

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

REMSTAR PLUS C-FLEX

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