Keystone/Halis/Dica/Lydia

FDA registration

SHANGHAI SANYOU MEDICAL CO. LTD·1 product·🇨🇳 China

Halis™ Lumbar Cage System, Lydia™ Anterior Lumbar Fusion System, Dica™ Direction Changeable Lumbar Cage System, KEYSTONE Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

PRO-TECH DESIGN & MFG., INC.

FDA registration

PRO-TECH DESIGN & MFG., INC.·2 products·🇺🇸 United States

SaberScope 5

FDA registration

ATL Technology CR Limitada·2 products·🇨🇷 Costa Rica

CardioCel Cardiovascular Patch

FDA registration

LEMAITRE VASCULAR, INC.·1 product·🇺🇸 United States

Saberscope

FDA registration

XENOCOR·2 products·🇺🇸 United States

Millennium

FDA UDI

Avalign Technologies, Inc.·00190776093907·Frazier Suction Tube, RoundHole

SignalHF

FDA registration

IMPLICITY·2 products·🇫🇷 France

VitreJect Syringe

FDA registration

OCUJECT, LLC·2 products·🇺🇸 United States

ROSSIX AB

FDA registration

ROSSIX AB·1 product·🇸🇪 Sweden

Saberscope5 Laparoscope

FDA 510(k)

FDA Class 2 ·Gastroenterology, Urology

CARDIOCEL

FDA 510(k)

FDA Class 2 ·Cardiovascular

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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

Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

FDA classification

FDA Class 2 ·Patch, Pledget And Intracardiac, Petp, Ptfe, Polypropylene

Laparoscope, General & Plastic Surgery

FDA classification

FDA Class 2 ·Laparoscope, General & Plastic Surgery