15 results · 28ms · 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.

DORNIER MEDILAS D 30 LASER, MEDILAS D 1064

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

K082959

FDA UDI
Unimed Medical Supplies, Inc.·06945664812412·SpO2 interface cable/Philips-Masimo/2.2M/309+12...

Unimed

FDA UDI
Unimed Medical Supplies, Inc.·06936735463947·One-piece ECG Monitor Cable Philips

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014608563·BERCHTOLD 4.25" DELUXE GEL

VERDICT -II BAR; VERDICT -II BZO

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

CRITERION 60 OR PM 60

FDA 510(k)
FDA Class 2 ·Anesthesiology

EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT-FULLY COVERED

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·March 25, 2015

EMAX 2 PLUS MOTOR

FDA Adverse Event
Malfunction ·THE ANSPACH EFFORT, INC.·Product code HBC·April 24, 2013

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·July 9, 2014

XP1 SINGLE SYSTEM DENTAL IMPLANT

FDA Adverse Event
Injury ·KEYSTONE DENTAL·Product code DZE·July 23, 2008

EVOLUTION BILIARY CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code FAD·March 12, 2015

EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Injury ·COOK IRELAND LTD·Product code ESW·November 12, 2014

EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code ESW·November 27, 2014

EVOLUTION ESOPHAGEAL CONTROLLED-RELEASE STENT - FULLY COVERED

FDA Adverse Event
Malfunction ·COOK IRELAND LTD·Product code ESW·November 24, 2014

Promote Quadra, Sterile EO, Model # / Part #: CD3221-36/100025054, 60019195; CD3223-36P/100013763; CD3239-40/100029115, 100029254, 100037181; CD3239-40Q/100029116, 100029244, 100037115

FDA Enforcement
Class II ·Terminated·St Jude Medical Inc.·July 4, 2018