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

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INDIKO

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

Sapphire 1100 35

FDA UDI
SIZEWISE RENTALS, L.L.C.·00845699000951·120V Sapphire 1100 35 Rev 1 and Rev 2

OsteoMed

FDA UDI
OSTEOMED LLC·00845694040068·PrimaLIF 5mm Kerrison Rongeur, Forward

LEONE SPA

FDA UDI
LEONE SPA·08033707096948·BKT 35 INTERACTIVE SL 22 T-22 BH

CORTICAL BONE SCREW 3.5mm x 35mm

FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665034110·

Cosmolock

FDA UDI
Kalitec Direct LLC·B07311K1100530·Caddie, 7.5mm Screws

MODEL VISULAS 532S LASER WITH THE VITE OPTION

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

IVS TUNNELLER

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

CORTICAL BONE SCREW, Ø3.5MM X 35MM

FDA Adverse Event
Malfunction ·ARTHREX, INC.·Product code HSB·October 3, 2022

WAVEWRITER ALPHA

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·July 14, 2023

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC SELF-EXPANDING NITINOL STENT SYSTEM

PARADIGM INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code LZG·May 13, 2013

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·September 23, 2014

GREENLIGHT ADDSTAT

FDA Adverse Event
Malfunction ·AMS, INNOVATION CENTER - SILICON VALLEY·Product code GEX·May 17, 2011

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC VASCULAR SELF-EXPANDING STENT SYSTEM

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC VASCULAR SELF EXPANDING STENT SYSTEM

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC VASCULAR SELF-EXPANDING STENT SYSTEM

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·Epic Vascular Self-Expanding Stent System

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·EPIC SELF-EXPANDING NITINOL STENT SYSTEM

Stent, Iliac

FDA Pre-Market Approval
FDA Class 3 ·Epic Self Expanding Stent System