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APEX-LNK ACETABULAR INSERT, E, APEX-LNK ACETABULAR INSERT, F, APEX-LNK

FDA 510(k)
FDA Class 2 ·Orthopedic

APEX-LNK POLY ACETABULAR CUP LINERS

FDA Adverse Event
Malfunction ·OMNLIFE SCIENCE, INC.·Product code LPH·April 4, 2012

N/A

FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·07613327487657·HoverMatt LINK 34" W x 78" L

HoverTech

FDA UDI
HYGIA HEALTH SERVICES, INC.·10817357022572·HoverTech HoverMatt LINK 39" W x 78" L

Single Patient Use HoverMatt

FDA UDI
Hovertech International·00816299011142·34" Single Patient Use HoverMatt LINK Breathable

HoverTech

FDA UDI
HYGIA HEALTH SERVICES, INC.·10817357022565·HoverTech HoverMatt LINK 34" W x 78" L

Single Patient Use HoverMatt

FDA UDI
Hovertech International·00816299011180·50" Single Patient Use HoverMatt LINK Breathable

N/A

FDA UDI
STRYKER SUSTAINABILITY SOLUTIONS, INC.·07613327487701·HoverMatt LINK 39" W x 78" L

Single Patient Use HoverMatt

FDA UDI
Hovertech International·00816299011166·39" Single Patient Use HoverMatt LINK Breathable

LnK Posterior Cervical Fixation System

FDA 510(k)
FDA Class 2 ·Orthopedic

LnK Anterior Cervical Plate System

FDA 510(k)
FDA Class 2 ·Orthopedic

QUICK SCREW DRIVER (C-SCREW)

FDA Adverse Event
Malfunction ·L&K BIOMED CO., LTD.·Product code NKG·October 27, 2021

LnK Cervical Interbody Fusion Cage System

FDA 510(k)
FDA Class 2 ·Orthopedic

LnK Cervical Interbody Fusion Cage System

FDA 510(k)
FDA Class 2 ·Orthopedic

LnK Lumbar Interbody Fusion Cage System

FDA 510(k)
FDA Class 2 ·Orthopedic

LnK Lumbar Interbody Fusion Cage System

FDA 510(k)
FDA Class 2 ·Orthopedic

APEX-LNK POLY ACETABULAR CUP LINERS

FDA 510(k)
FDA Class 2 ·Orthopedic

APEX-LNK POLY ACETABULAR CUP LINERS

FDA Adverse Event
Malfunction ·OMNILIFE SCIENCE INC.·Product code LPH·February 13, 2012

APEX-LNK POLY ACETABULAR CUP LINERS

FDA Adverse Event
Malfunction ·OMNILIFE SCIENCE INC.·Product code LPH·February 13, 2012

APEX-LNK POLY ACETABULAR CUP LINERS

FDA Adverse Event
Malfunction ·OMNLIFE SCIENCE, INC·Product code LPH·April 4, 2012