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

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NAVITRACK SYSTEM-FLUOROSPINE, MODEL 900.005

FDA 510(k)
FDA Class 2 ·Neurology

ACE

FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950013449·ACE TWO WAY PLASTIC AUTOMATIC VALVE STERILE DIS...

n/a

FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM50311561·Device for prosthetic application (impression, ...

PHOENIX HEMODIALYSIS DELIVERY SYSTEM, GAMBRO CARTRIDGE FOR HEMODIALYSIS BLOOD TUBING SET

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

BCI 3403 SLEEP SCREENING PULSE OXIMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

9616240-2006-00341

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

9616240-2006-00332

FDA Adverse Event
Other ·Product code FII·June 1, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

9616240-2006-00339

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00340

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00350

FDA Adverse Event
Malfunction ·Product code FII·June 23, 2006

9616240-2006-00345

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

MARKERS

FDA Adverse Event
Malfunction ·PRAXIM·Product code HAW·January 3, 2007

CADD MEDICATION CASSETTE

FDA Adverse Event
Malfunction ·NULL·Product code FPA·February 4, 2022

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

UNKNOWN ZIMMER HUMERAL TRIAL INSTRUMENT

FDA Adverse Event
Injury ·ZIMMER, INC.·Product code LXH·March 22, 2011

ARTEGRAFT COLLAGEN VASCULAR GRAFT

FDA Adverse Event
Malfunction ·ARTEGRAFT, INC.·Product code LXA·June 23, 2006

GORE EXCLUDER AAA ENDOPROSTHESIS

FDA Adverse Event
Injury ·W. L. GORE & ASSOCIATES, INC.·Product code MIH·April 16, 2008

HEALICOIL RSB SA 4.75MM W/1 UT & 1 UB BK-- Absorbable Suture anchor Product Number: 72203705

FDA Enforcement
Class II ·Ongoing·Smith & Nephew, Inc.·October 28, 2020