5,634 results · 25ms · Sources: EU EUDAMED, US FDA

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K2M, Inc.

Manufacturer
🇺🇸 United States·1 Importer

K2M, INC.

FDA registration
K2M, INC.·46 products·🇺🇸 United States

dental diamond bur

FDA UDI
STRAUSS & CO - INDUSTRIAL DIAMONDS LTD·D877K2M6·Dental Diamond Bur

GM-K2 M

Device
EU MDR · Eu Md Class 1 ·PATELLA-96 Kereskedelmi és Szolgáltató Korlátolt Felelősségű Társaság·On the market

K2M COCR ROD

FDA 510(k)
FDA Class 2 ·Orthopedic

K2M MODULAR HOOKS

FDA 510(k)
FDA Class 2 ·Orthopedic

K2M Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

K2M Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

K2M COCR WIRE

FDA 510(k)
FDA Class 2 ·Orthopedic

K2M Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

K2M Expandable Interbody System

FDA 510(k)
FDA Class 2 ·Orthopedic

K2M Growing Spine System

FDA 510(k)
FDA Class 2 ·Orthopedic

K2M Fenestrated Tap System

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

K2M Patient Specific Rods

FDA 510(k)
FDA Class 2 ·Orthopedic

Brainlab Compatible K2M Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

K2M, PYRENEES CERVICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Brainlab Compatible K2M Navigation Instruments

FDA 510(k)
FDA Class 2 ·Neurology

K2M GEARSHIFT

FDA Adverse Event
Malfunction ·K2M, INC.·Product code MAX·May 30, 2018

EVEREST ® SPINAL SYSTEM

FDA Adverse Event
Malfunction ·STRYKER-SPINE·Product code LXH·September 9, 2019

K2M NAVIGATION INSTRUMENTS

FDA Adverse Event
Malfunction ·K2M, INC.·Product code OLO·November 16, 2017