Footswitch (7-PG1-132)

FDA registration

CREO MEDICAL LTD·1 product·🇬🇧 United Kingdom

Aortic Stent

FDA Pre-Market Approval

FDA Class 3 ·Minima Stent System

Baby Gorilla/Gorilla Plating System

FDA UDI

PARAGON 28, INC.·00889795039965·LCF Joint Preparation Paddle

DynaNail Removal Tool, Slap Hammer

FDA UDI

Medshape, Inc.·M97022002400030·

neXus

FDA UDI

MISONIX, INC.·00841626102880·neXus SonaStar® Short Housing

Tap, Quick Connect, Reusable, Helical Ridge

FDA UDI

Medshape, Inc.·M9702400030000·

Aortic Stent

FDA Pre-Market Approval

FDA Class 3 ·Minima Stent System

VERTEBRON SCP CERVICAL PLATE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

COROENT SMALL INTERBODY SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Wingman

FDA UDI

STRYKER CORPORATION·07613327061284·Tube Set/Activation Button for Scope Holder, Do...

Minima Stent System

FDA registration

RENATA MEDICAL·2 products·🇺🇸 United States

Minima; Minima Growth Stent; Minima Stent; Minima Stent System; Minima System

FDA registration

MEDICAL MURRAY, INC.·1 product·🇺🇸 United States

Gibralt

FDA UDI

Choice Spine, LP·10885862145109·

Aortic Stent

FDA Pre-Market Approval

FDA Class 3 ·Minima Stent System

Aortic Stent

FDA Pre-Market Approval

FDA Class 3 ·Minima Stent System

Aortic Stent

FDA classification

FDA Class 3 ·Aortic Stent

Intervertebral Fusion Device With Bone Graft, Cervical

FDA classification

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

Appliance, Fixation, Spinal Intervertebral Body

FDA classification

FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body

FMD-005-5060-02 F.O SINGLE USE MACINTOSH BLADE (PH) SIZE 2 (NON- STERILE)

FDA registration

S.G. MANUFACTURERS·1 product·🇵🇰 Pakistan