EARP Nerve Cuff Electrode

FDA registration

RETROPSOAS TECHNOLOGIES, LLC·1 product·🇺🇸 United States

EARP Cuff

FDA registration

ARDIEM MEDICAL, INC.·1 product·🇺🇸 United States

EARP Nerve Cuff Electrode

FDA 510(k)

FDA Class 2 ·Ear, Nose, Throat

Stimulator, Nerve

FDA classification

FDA Class 2 ·Stimulator, Nerve

Unicon (Etafilcon A) Soft (hydrophilic) Contact Lens with UV Blocker for Daily Wear

FDA registration

UNICON OPTICAL CO., LTD.·2 products·🇹🇼 Taiwan

zonedin 58 monthly contact lens

FDA registration

ZONEDIN VISION LLC·2 products·🇺🇸 United States

CarboFix Plate System

FDA registration

CarboFix Orthopedics, Ltd.·3 products·🇮🇱 Israel

LEONE SPA

FDA UDI

LEONE SPA·08033707040606·DB BRACKETS 22 H/W T-22 BH 2nd BIC L/L

Epredia E1000 Dx Digital Pathology Solution

FDA registration

SHANDON DIAGNOSTICS LIMITED·3 products·🇬🇧 United Kingdom

WELLlife™ COVID-19 Antigen Home Test

FDA registration

GUANGZHOU WONDFO BIOTECH CO., LTD.·1 product·🇨🇳 China

Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

Hough™ COVID-19 Antigen Home Test

FDA registration

WONDFO USA CO., LTD.·1 product·🇺🇸 United States

RUETSCHI TECHNOLOGY AG

FDA registration

RUETSCHI TECHNOLOGY AG·1 product·🇨🇭 Switzerland

UNICON (ETAFILCON A) SOFT (HYDROPHILIC) CONTACT LENS WITH UV BLOCKER FOR DAILY WEAR

FDA 510(k)

FDA Class 2 ·Ophthalmic

PLASIATEK ACTUATOR

FDA 510(k)

FDA Class 2 ·Anesthesiology

Tube, Tracheal (W/Wo Connector)

FDA classification

FDA Class 2 ·Tube, Tracheal (W/Wo Connector)

Lenses, Soft Contact, Daily Wear

FDA classification

FDA Class 2 ·Lenses, Soft Contact, Daily Wear