25 results · 27ms · Sources: EU EUDAMED, US FDA

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Materialise Shoulder System™, Materialise Shoulder Guide and Models, SurgiCase Shoulder Planner

FDA 510(k)
FDA Class 2 ·Orthopedic

Eye Pads - 25/Box

FDA UDI
Certified Safety Manufacturing, Inc.·00766588311128·Eye Pads - 25/Box

X SERIES

FDA UDI
Zoll Medical Corporation·00847946060367·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 3/5 L...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946029616·X SERIES ADVANCED, 12 LEAD W/INTERP, PACE, SPO2...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946062033·X SERIES ADVANCED, MONITOR/DEFIBRILLATOR, 12 LE...

X SERIES

FDA UDI
Zoll Medical Corporation·00847946030155·X SERIES ADVANCED, 3/5 LEAD, PACE, SPO2, SPCO, ...

AC3 IABP, AC3 Optimus IABP, AutoCAT2 Wave IABP, AutoCAT2 IABP

FDA 510(k)
FDA Class 2 ·Cardiovascular

LIMACORPORATE SMR CTA HUMERAL HEADS

FDA 510(k)
FDA Class 2 ·Orthopedic

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523145072·R CR UHMWPE Congruent Tibial Insert Sz A 12mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523102174·R CR MAXTM HXL Congruent Tibial Insert Sz A 12mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523172375·CR Tibial Insert Trial with Posterior Pin Relie...

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523124411·R CR Tibial Insert Trial Sz A 12mm

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523101405·R CR E-MAXTM Vitamin E Congruent Tibial Insert ...

ImmunoCAP Tryptase Curve Control 1

FDA UDI
Phadia AB·07333066011998·ImmunoCAP Tryptase Curve Control 1

Kyocera Medical Technologies, Inc.

FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523165582·R CR Tibial Insert Trial with Anterior Slot, Sz...

DEXCOM ONE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code QBJ·September 10, 2024

ACTIVA

FDA Adverse Event
Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·May 9, 2012

TUBE, GASTROINTESTINAL (AND ACCESS)

FDA Adverse Event
Malfunction ·C. R. BARD INC. (BASD)·Product code KNT·November 11, 2008

RESTORE ULTRA

FDA Adverse Event
Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·August 26, 2011

HIRES 90K IMPLANT

FDA Adverse Event
Malfunction ·ADVANCED BIONICS, LLC·Product code MCM·July 12, 2013