VISIONAIRE

FDA registration

SMITH & NEPHEW, INC.·4 products·🇺🇸 United States

VISIONAIRE

FDA registration

Smith & Nephew, Inc.·4 products·🇺🇸 United States

VISIONAIRE

FDA registration

Smith & Nephew, Inc.·4 products·🇺🇸 United States

VISIONAIRE UK Patient Matched Cutting Guides

FDA 510(k)

FDA Class 2 ·Orthopedic

Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

FDA classification

FDA Class 2 ·Prosthesis, Knee, Femorotibial, Non-Constrained, Cemented, Metal/Polymer

MEDI

FDA UDI

MEDI MANUFACTURING, INC.·00636257073414·PROTECT PATELLA TRACKING BRACE, LT, MD

VITA TITANKERAMIK

FDA UDI

Vita - Zahnfabrik H. Rauter Gesellschaft mit beschränkter Haftung & Co Kommanditgesellschaft·J017B2115120·VITA TITANKERAMIK INTENSIVE, IN5, 12 g

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776199494·SAYEREDDICK KNOT PUSHER CLOSED

Thompson MIS BoneBac TPLIF

FDA registration

THOMPSON MIS·1 product·🇺🇸 United States

ROMD, LLC

FDA registration

ROMD, LLC·1 product·🇺🇸 United States

Bio-logic Scout Sport

FDA registration

NATUS MEDICAL INCORPORATED DBA EXCEL-TECH LTD. (XLTEK)·1 product·🇨🇦 Canada

InvisiShunt

FDA registration

Longeviti Neuro Solutions·1 product·🇺🇸 United States

DERMABOND™ PRINEO™ Skin Closure System (22cm)

FDA registration

ETHICON, INC.·1 product·🇺🇸 United States

DERMABOND™ PRINEO™ Skin Closure System (22cm)

FDA registration

ETHICON, INC.·1 product·🇺🇸 United States

ALEUTIAN® Interbody Systems

FDA UDI

K2M, INC.·10888857308060·Parallel Rasp, Size 18x45x17 mm

MMODIFICATION TO LAMINARIA

FDA 510(k)

FDA Class 2 ·Obstetrics/Gynecology

BONEBAC T-PLIF INTERVERTEBRAL BODY FUSION DEVICE SYSTEM

FDA 510(k)

FDA Class 2 ·Orthopedic

Dilator, Cervical, Hygroscopic-Laminaria

FDA classification

FDA Class 2 ·Dilator, Cervical, Hygroscopic-Laminaria

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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