DIO SM Implant System

FDA registration

DIO Corporation·2 products·🇰🇷 South Korea

DIO SM IMPLANT SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

ACCESSORIES, SOFT LENS PRODUCTS

FDA registration

GO PRO NOW LTD·1 product·🇬🇧 United Kingdom

CooperVision, Inc.

FDA registration

CooperVision, Inc.·1 product·🇺🇸 United States

Prosthesis Esophageal

FDA registration

BBF STERILISATIONSSERVICE GMBH·1 product·🇩🇪 Germany

SMHP Lens Cleaning and Disinfecting Solution, 12oz

FDA registration

K. C. PHARMACEUTICALS, INC.·1 product·🇺🇸 United States

SchureMed

FDA UDI

SCHUERCH CORPORATION·00810014606217·BARIATRIC STIRRUP BOOT PADS

SchureMed

FDA UDI

SCHUERCH CORPORATION·00810014603636·Bariatric Boot Pads (pair)

PRISMAFLEX M150

FDA registration

STERLAB·1 product·🇫🇷 France

Effective Cap

FDA registration

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

SAUFLON MULTI LENS CARE SYSTEM

FDA 510(k)

FDA Class 2 ·Ophthalmic

RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEM

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

Prosthesis, Esophageal

FDA classification

FDA Class 2 ·Prosthesis, Esophageal

Implant, Endosseous, Root-Form

FDA classification

FDA Class 2 ·Implant, Endosseous, Root-Form

Accessories, Soft Lens Products

FDA classification

FDA Class 2 ·Accessories, Soft Lens Products