PRO-TECH DESIGN & MFG., INC.

FDA registration

PRO-TECH DESIGN & MFG., INC.·1 product·🇺🇸 United States

NeuroPace Burr Hole Cover

FDA registration

NEUROPACE·1 product·🇺🇸 United States

NeuroPace® Burr Hole Cover

FDA registration

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

NEUROPACE BURR HOLE COVER MODEL 8110

FDA 510(k)

FDA Class 2 ·Neurology

Cover, Burr Hole

FDA classification

FDA Class 2 ·Cover, Burr Hole

Penumbra System MAX

FDA registration

Penumbra Inc.·1 product·🇺🇸 United States

Penumbra System (Reperfusion Catheters, Separators, Aspiration Tubing, and 3D Revascularization Device)

FDA registration

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

Penumbra System MAX

FDA registration

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

Sterigenics UK Limited

FDA registration

Sterigenics UK Limited·1 product·🇬🇧 United Kingdom

Penumbra System MAX

FDA registration

Penumbra Inc.·1 product·🇺🇸 United States

Penumbra System MAX

FDA registration

Penumbra Inc.·1 product·🇺🇸 United States

CATHETER, THROMBUS RETRIEVER

FDA registration

CARDIMED ASIA MEDIKAL SANAYI VE TICARET LTD STI·1 product·🇹🇷 Türkiye

Schneider ASR B.V.

FDA registration

Schneider ASR B.V.·1 product·🇳🇱 Netherlands

SmartGuard Elite

FDA registration

SMARTGUARD RX INC·2 products·🇺🇸 United States

OralID

FDA registration

FORWARD SCIENCE TECHNOLOGIES LLC·1 product·🇺🇸 United States

LIQUISHIELD-S (0.7G), MODEL LS 0010, LIQUISHIELD-S (2.0G), MODEL LS 0020

FDA 510(k)

FDA Class 1 ·General Hospital

PENUMBRA SYSTEM MAX

FDA 510(k)

FDA Class 2 ·Cardiovascular

Catheter, Thrombus Retriever

FDA classification

FDA Class 2 ·Catheter, Thrombus Retriever

Bandage, Liquid

FDA classification

FDA Class 1 ·Bandage, Liquid