Bigfoot Unity Diabetes Management System- For Humalog-Lispro-Lyumjev and Toujeo Max Only

FDA registration

BIGFOOT BIOMEDICAL, INC.·2 products·🇺🇸 United States

Bigfoot Unity Diabetes Management System

FDA 510(k)

FDA Class 2 ·Clinical Chemistry

Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems

FDA classification

FDA Class 2 ·Integrated Continuous Glucose Monitoring System, Factory Calibrated, Not For Use With Automated Insulin Delivery Systems

K201145

FDA registration

EXEL INC. DBA DHL SUPPLY CHAIN (USA)·1 product·🇺🇸 United States

CATHETER, EMBOLECTOMY Over-the-Wire Catheter

FDA registration

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

OVER-THE-WIRE EMBOLECTOMY CATHETER

FDA registration

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

X-Pac Expandable Cage System

FDA registration

Expanding Innovations, Inc.·1 product·🇺🇸 United States

Tissue Holder

FDA UDI

KATENA PRODUCTS, INC.·00841668112847·BARRON ARTIFICIAL ANTERIOR CHAMBER

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112748·BARRON VACUUM PUNCH 7.25MM

Mediflex Laparoscopic Instruments - Needle Holders

FDA UDI

FLEXBAR MACHINE CORPORATION·00842102112140·Modular Needle Holder w/Radel Handle, 5mm x 45...

Fluid Retention Ring

FDA UDI

KATENA PRODUCTS, INC.·00841668112854·VIDAURRI FLUID RETENTION WELL 8.7MM

Mediflex Laparoscopic Instruments - Needle Holders

FDA UDI

FLEXBAR MACHINE CORPORATION·00842102112157·Ins for Mod Needle Holder, Straight Jaw

Ring probe (2021) 45°, 30 x 36mm

Device

EU MDR · Eu Md Class 2a ·Varian Medical Systems, Inc.·On the market·26 countries

X-Pac Expandable Lumbar Cage System

FDA 510(k)

FDA Class 2 ·Orthopedic

OVER THE WIRE EMBOLECTOMY CATHETER, MODEL 2302

FDA 510(k)

FDA Class 2 ·Cardiovascular

Ring probe (2021) 45°, 26 x 32 mm

Device

EU MDR · Eu Md Class 2a ·Varian Medical Systems, Inc.·On the market·26 countries

Catheter, Embolectomy

FDA classification

FDA Class 2 ·Catheter, Embolectomy

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA classification

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