26 results · 22ms · Sources: EU EUDAMED, US FDA

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COMPETITOR UNICONDYLAR KNEE TIBIAL BASEPLATE

FDA 510(k)
FDA Class 2 ·Orthopedic

Catalyft PL Expandable Interbody System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000253615·AUGER 6061011 AUGER

Straight Plate, 11-Hole

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665027174·

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193104300·HA PEEK EVOS Curved, , 11mmx11mmx 30mm , FLAT 6...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523177905·Tesera-k Cervical Interbody Instrument Case Tray 1

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170739·Tk C, Solid Ball U-Jointed Screwdriver - Micro

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170685·Tk C, Retaining Straight Screwdriver - Micro

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523177912·Tesera-k Cervical Interbody Instrument Case Tray 2

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170722·Tk C, Retaining Ball U-Jointed Screwdriver - Micro

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523177899·Tesera-k Cervical Interbody Instrument Case

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523170692·Tk C, Solid Straight Screwdriver - Micro

LIGASURE 5MM LAPAROSCOPIC SEALER-DIVIDER, MODEL LS1500

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

LIVESURE MORPHINE SCREEN TEST

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·October 16, 2013

ST JOSEPHS PHOENIX, AZ 1

FDA Adverse Event
Malfunction ·SORIN GROUP USA·Product code DWF·July 31, 2009

RU NOVOSIBRIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DTZ·April 11, 2013

RU NOVOSIBIRSK

FDA Adverse Event
Other ·SORIN GROUP ITALIA·Product code DWF·October 16, 2013

CP87170 DE MUENCHEN

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DTZ·July 15, 2011

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·April 16, 2013

PRECISE OTW NITINOL STENT

FDA Adverse Event
Malfunction ·CORDIS DE MEXICO·Product code NIM·June 12, 2008