Millstone Medical Outsourcing LLC

FDA registration

Millstone Medical Outsourcing LLC·3 products·🇺🇸 United States

Cross-Fuse II PEEK IBF System

FDA registration

Xtant Medical Holdings, Inc.·3 products·🇺🇸 United States

PIONEER CROSSFUSE II IBF/VBR SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

CF Carbon Fiber Post

FDA registration

J. MORITA USA, INC.·1 product·🇺🇸 United States

MS53i2 (ML21053)

FDA registration

JVCKENWOOD Corporation·1 product·🇯🇵 Japan

Disc Prep

FDA UDI

Life Spine, Inc.·00190837089900·

Kitazato IUI Catheter with Stainless Steel Center Core Type, 7 cm, model number Type 1-v2

FDA registration

KITAZATO CORPORATION·1 product·🇯🇵 Japan

Sterigenics U.S., LLC

FDA registration

Sterigenics U.S., LLC·1 product·🇺🇸 United States

Virtue Male Sling System with Alexis Wound Retractor

FDA registration

COLOPLAST MANUFACTURING US, LLC·2 products·🇺🇸 United States

CARBON POST

FDA 510(k)

FDA Class 1 ·Dental

POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS

FDA 510(k)

FDA Class 3 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

Post, Root Canal

FDA classification

FDA Class 1 ·Post, Root Canal

Automated External Defibrillators (Non-Wearable)

FDA classification

FDA Class 3 ·Automated External Defibrillators (Non-Wearable)