Spineology5627 (LN) - Duo Lumbar Interbody Fusion Device

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Duo Lumbar Interbody Fusion Device

FDA registration

SPINEOLOGY INC.·1 product·🇺🇸 United States

Rampart D Lumbar Interbody Fusion Device

FDA 510(k)

FDA Class 2 ·Orthopedic

VIVID POST DRILL

FDA UDI

BIOLOREN SRL·08056099233302·Conical drill ø 1.2 - 1.65 mm.

Interlink System T Connector Ext Se

FDA registration

Baxter Healthcare of Puerto Rico LLC·1 product·🇺🇸 United States

Interlink System T Connector Ext Se

FDA registration

BAXTER HEALTHCARE CORPORATION·1 product·🇺🇸 United States

Interlink System T Connector Ext Se

FDA registration

Baxter Limited·1 product·🇲🇹 Malta

HYGECHROMA

FDA registration

HYGEDENT INC.·1 product·🇨🇳 China

Hayden Medical

FDA UDI

Hayden Medical, Inc.·00840319720981·Metzenbaum Needle Holder 7-1/4" (18.4cm), stra...

Allday Dry Mouth Spray

FDA registration

ELEVATE ORAL CARE, LLC·1 product·🇺🇸 United States

MoMe Kardia Monitor

FDA registration

Validic Logistics, LLC·2 products·🇺🇸 United States

TURNER MEDICAL INC.

FDA registration

TURNER MEDICAL INC.·1 product·🇺🇸 United States

MoMe Kardia

FDA registration

INFOBIONIC, INC.·2 products·🇺🇸 United States

POWDER FREE VINYL PATIENT EXAMINATION GLOVES, COLORED (YELLOW)

FDA 510(k)

FDA Class 1 ·General Hospital

INTERLINK SYSTEM-T-CONNECTOR EXTENSION SET, MODEL 2N3326

FDA 510(k)

FDA Class 2 ·General Hospital

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Vinyl Patient Examination Glove

FDA classification

FDA Class 1 ·Vinyl Patient Examination Glove

Set, Administration, Intravascular

FDA classification

FDA Class 2 ·Set, Administration, Intravascular