27 results · 21ms · Sources: EU EUDAMED, US FDA

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Embrella Endoscopic Distal Attachment

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

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000868062·PLATE 6190030 ANTERIOR CERVICAL 30MM

ATLANTIS® Anterior Cervical Plate System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994235824·PLATE 6190030 ANTERIOR CERVICAL 30MM

Greenwald Surgical Company, Inc.

FDA UDI
GRACE MANUFACTURING, INC.·10801334008932·Otis Bougie-a-Boule. Mirror finish, stainless s...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694041003·3.0mm x 0 Degree ExtremiFuse Implant

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690189701·AK3 Patella Medial Hole Drill Guide

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·ActaStim-S Spine Fusion Stimulator

OsteoMed

FDA UDI
OSTEOMED LLC·00845694069960·ExtremiFuse 3.0mm 0 Degree Implant Sterile Qty 5

NA

FDA UDI
STRYKER CORPORATION·04546540373212·6.0mm Acorn

NA

FDA UDI
STRYKER CORPORATION·04546540373229·7.5mm Acorn

NA

FDA UDI
STRYKER CORPORATION·04546540373236·9.0mm Acorn

EXPECT ENDOSCOPIC ASPIRATION NEEDLE

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

TAPERLOC COMPLETE SIZE 4MM AND XR 123

FDA 510(k)
FDA Class 2 ·Orthopedic

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·ActaStim-S Spine Fusion Stimulator

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·ActaStim-S Non Invasive Spine Fusion Stimulator

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·ActaStim-S Spine Fusion Stimulator

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 2 ·ActaStim-S

7900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS GMBH·Product code JAA·June 18, 2013

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·August 4, 2011

HEARTSTART FRX

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·September 18, 2014