23 results · 24ms · Sources: EU EUDAMED, US FDA

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EQUIVITAL

FDA 510(k)
FDA Class 2 ·Cardiovascular

MSI Precision Specialty Instruments

FDA UDI
Med Saver, Inc.·00194613017712·K-Wire, Double Ended, Trocar Point, Diameter Si...

Prosplints

FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357130542·

5.0MM VARIABLE ANGLE LOCKNG SCREW/SLF-TPNG/STRDRV/65MM

FDA Adverse Event
Injury ·SYNTHES MEZZOVICO·Product code JDP·August 28, 2015

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K1100540·Caddie, 8.5mm Screws

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·January 26, 2015

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·March 2, 2015

IMPLANT, FIXATION DEVICE CONDYLAR PLATE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code JDP·February 23, 2017

PERIOPATCH

FDA 510(k)
FDA Unclassified ·Unknown

KONICA DIRECT DIGITIZER REGIUS MODEL 350

FDA 510(k)
FDA Class 2 ·Radiology

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

LOCKING CAP

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code KTT·October 19, 2012

IMPLANT, FIXATION DEVICE, CONDYLAR PLATE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code JDP·June 1, 2015

3085SP SURGICAL TABLE

FDA Adverse Event
STERIS CORPORATION - MONTGOMERY·Product code FQO·June 3, 2011

MBT CEM KEEL TIB TRAY SZ3

FDA Adverse Event
Injury ·9616671 DEPUY (IRELAND)·Product code NJL·May 15, 2013

POWERED WHEELCHAIR

FDA Adverse Event
Malfunction ·UNKNOWN·Product code ITI·September 24, 2014

BD Q-SYTE¿ EXTENSION SET

FDA Adverse Event
Malfunction ·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FPA·April 20, 2022

Ethicon Stratafix Symmetric PDS Plus Knotless Tissue Control Device Ethicon LLC Guaynabo, Puerto Rico 00969. Intended for general soft tissue approximation where use of an absorbable suture is appropriate.

FDA Enforcement
Class II ·Terminated·Ethicon, Inc.·December 18, 2013