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

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CORVIS ST

FDA 510(k)
FDA Class 2 ·Ophthalmic

AQUILION PRIME

FDA 510(k)
FDA Class 2 ·Radiology

HX-5/6-1 ENDOSCOPIC CLIPPING DEVICE

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

LINER: VERSAFITCUP DM DOUBLE MOBILITY HC LINER Ø 54/28

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code MEH·June 14, 2022

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

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

9800

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

APD 60.000 RPM

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HBB·September 24, 2014

TOTAL ASR FEM IMP SIZE 49

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, 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

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

FDA Adverse Event
Malfunction ·RESPIRONICS, INC·Product code BZD·July 30, 2021

REMSTAR AUTOA-FLEX W/ HUM, SYSONE 60SRS, AUS

FDA Adverse Event
Injury ·RESPORINOC INC·Product code BZD·August 11, 2021