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

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ACQA

FDA 510(k)
FDA Class 2 ·Radiology

5530 3L SYRINGE

FDA UDI
HANS RUDOLPH, INC.·00817136020822·5530 3L CALSYR W/TRPL-V OUTLET

WET LIGHT PERSONAL MOISTURIZER

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

DYNAREX INTERMITTENT CATHETERS, MALE, FEMALE, PEDIATRIC

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

DAVOL ABSORBABLE FASTENER SYSTEM, MODEL (S) 0113080,0113081, 0113082, 0113084, 0113086, 0113087

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

REMSTAR AUTO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

REMSTAR PRO

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·August 20, 2021

REMSTAR AUTO A-FLEX W/HUMID

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code BZD·August 10, 2021

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

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

DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·May 9, 2025

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

FDA Adverse Event
Injury ·RESPIRONICS INC·Product code BZD·August 30, 2021

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

IMPAX CV OUTBOUND (RESULTS MANAGEMENT 2.08)

FDA Adverse Event
Malfunction ·AGFA HEALTHCARE·Product code LLZ·February 28, 2014

STENOSCOP

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 9, 2013

PINNACLE MTL INS NEUT36IDX52OD

FDA Adverse Event
Injury ·DEPUY INTL., LTD.·Product code KWA·May 18, 2011

REMSTAR PRO C-FLEX+

FDA Adverse Event
Malfunction ·RESPIRONICS INC·Product code BZD·February 8, 2022

REMSTAR AUTO A-FLEX

FDA Adverse Event
Malfunction ·RESPIRONICS, INC.·Product code BZD·January 14, 2022

REMSTAR AUTO A-FLEX W/SD CARD, GER

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

REMSTAR AUTO W/HT HUM,SYS ONE,60 SRS,CAN

FDA Adverse Event
Injury ·RESPIRONICS, INC.·Product code BZD·August 3, 2021

U BY KOTEX SLEEK

FDA Adverse Event
Malfunction ·K-C AFC MANUFACTURING, S. DE R.L. DE C.V·Product code HEB·August 31, 2018