13 results · 29ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

KEMTROL SERUM CONTROL-NORMAL CAT NO. 7024

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

IPL Hair Removal

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

BAUSCH & LOMB SOFLENS MULTIFOCAL (POLYMACON) VISIBILITY TINTED CONTACT LENS

FDA 510(k)
FDA Class 2 ·Ophthalmic

TROCHANTERIC NAIL KIT, TI GAMMA3 11X180MM X 130

FDA Adverse Event
Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 17, 2012

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·February 27, 2009

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·February 27, 2009

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·February 27, 2009

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·February 27, 2009

ULTRAFLEX PRECISION COLONIC STENT SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC IRELAND, LTD.·Product code MQR·February 27, 2009

TELIGEN

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 17, 2013

TERUMO ADVANCE PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·November 8, 2010

RIATA PASSIVE FIXATION

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVY·July 8, 2014

NAVISTAR RMT THERMOCOOL

FDA Adverse Event
Injury ·BIOSENSE WEBSTER INC·Product code OAD·August 29, 2025