IS-III active System_S-narrow Type

FDA registration

NEOBIOTECH CO., LTD.·2 products·🇰🇷 South Korea

IS-III active System_S-narrow Type

FDA 510(k)

FDA Class 2 ·Dental

Sync-Rx System

FDA registration

Volcano Corporation·1 product·🇺🇸 United States

Sync-Rx System

FDA registration

VOLCANO CORPORATION·1 product·🇺🇸 United States

PrestoDR 4343

FDA registration

CMT MEDICAL TECHNOLOGIES, LTD.·1 product·🇮🇱 Israel

Pre-Finisher

FDA UDI

TP ORTHODONTICS INC·00192029042571·Asian Non-Extraction

ScanX Barrier Envelope: G8511-0, G8511-1, G8511-2, G8511-2k, G8511-3, G8511-4

FDA registration

MACO BAG CORP.·1 product·🇺🇸 United States

Synchro2 Support Guidewire

FDA registration

Stryker Neurovascular·2 products·🇺🇸 United States

SYNC-RX SYSTEM, MODEL AS00010

FDA 510(k)

FDA Class 2 ·Radiology

MODIFICATION TO: NANOCROSS 0.14 OTW PTA DILATATION CATHETER, MODELS AB14W020210090, AB14W020210150

FDA 510(k)

FDA Class 2 ·Cardiovascular

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

System, X-Ray, Angiographic

FDA classification

FDA Class 2 ·System, X-Ray, Angiographic

Catheter, Percutaneous

FDA classification

FDA Class 2 ·Catheter, Percutaneous