Superhawk

FDA registration

RESPONSIVE ARTHROSCOPY·1 product·🇺🇸 United States

Protech3048 (TM) - Superhawk

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112885·CORNEAL TREPHINE BLADE6.75MM

Responsive Arthroscopy Suture Anchor System

FDA 510(k)

FDA Class 2 ·Orthopedic

SprintRay Apex Base - Light Pink - 1 Kg

FDA UDI

Sprintray, Inc.·00850039704659·APEX Base resin is a light-curable polymerizabl...

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112724·BARRON VACUUM PUNCH 6.75MM

Ultrasonic Nebulizer, Model: NE-520

FDA registration

HONG KONG LANLI TECHNOLOGY CO., LIMITED·1 product·🇭🇰 Hong Kong

ULTRASONIC NEBULIZER, MODEL NE-520

FDA registration

HENGSHENG INDUSTRY CO., LIMITED·1 product·🇭🇰 Hong Kong

BladderScan® BVI 6400

FDA registration

Verathon Inc.·2 products·🇺🇸 United States

Ultrasonic Nebulizer, Model: NE-520

FDA registration

KAM KIN LIMITED·1 product·🇭🇰 Hong Kong

Ultrasonic Nebulizer - Portable Nebulizer, Nebulizers, Rechargeable Nebulizer Machine for Adults and Kids

FDA registration

Fainteer Limited·1 product·🇺🇸 United States

Spriek Portable Nebulizer, Smart Digital Display Portable Nebulizer for Adults and Kids

FDA registration

PANY MED INC·1 product·🇺🇸 United States

Corneal Trephine

FDA UDI

KATENA PRODUCTS, INC.·00841668112823·BARRON VACUUM PUNCH 9.25MM

Pulse Oximeter, model: AOJ-70C

FDA registration

Guangzhou Berrcom Medical Device Co., Ltd·1 product·🇨🇳 China

Tisuthes e-PTFE Surgical Patch

FDA registration

SHANGHAI SUOKANG MEDICAL IMPLANTS CO., LTD.·2 products·🇨🇳 China

actiTENS iOS app, actiTENS Android app, actiTENS standard kit, actiTENS spare, Charging Case spare,self-adhesive strip

FDA registration

STIPLASTICS·4 products·🇫🇷 France

BLADDERSCAN BVI 6100

FDA 510(k)

FDA Class 2 ·Radiology

ULTRASONIC NEBULIZER, MODEL NE-520

FDA 510(k)

FDA Class 2 ·Anesthesiology

Fastener, Fixation, Nondegradable, Soft Tissue

FDA classification

FDA Class 2 ·Fastener, Fixation, Nondegradable, Soft Tissue

Nebulizer (Direct Patient Interface)

FDA classification

FDA Class 2 ·Nebulizer (Direct Patient Interface)