InBody 230

FDA registration

InBody Co, Ltd.·1 product·🇰🇷 South Korea

BIOSPACE BODY COMPOSITION ANALYZERS, MODEL INBODY 230

FDA 510(k)

FDA Class 2 ·Cardiovascular

Analyzer, Body Composition

FDA classification

FDA Class 2 ·Analyzer, Body Composition

"Catheter, Percutaneous Profiler PTA Balloon Catheter

FDA registration

Sterigenics U.S., LLC·2 products·🇺🇸 United States

Sklar

FDA UDI

SKLAR CORPORATION·10649111107054·ADAPTER F. (06-1201 LEFF)

Dimension(r) Reaction Vessels

FDA registration

Carclo Technical Plastics - Latrobe·58 products·🇺🇸 United States

Analyzer

FDA registration

Diamond Diagnostics Inc.·59 products·🇭🇺 Hungary

Reprocessed Unipolar Laparoscopic/Endoscopic Instruments

FDA registration

Stryker Sustainability Solutions·1 product·🇺🇸 United States

IMMULITE Albumin

FDA registration

Siemens Healthcare Diagnostics Inc.·59 products·🇺🇸 United States

IMMULITE Albumin

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·59 products·🇬🇧 United Kingdom

IMMULITE Albumin

FDA registration

SIEMENS HEALTHCARE DIAGNOSTICS INC.·59 products·🇺🇸 United States

Reprocessed Unipolar Laparoscopic/Endoscopic Instruments

FDA registration

Stryker Sustainability Solutions Lakeland·1 product·🇺🇸 United States

IMMULITE Albumin

FDA registration

Siemens Healthcare Diagnostics Inc.·59 products·🇺🇸 United States

Immulite Analyzer

FDA registration

SCIENTIFIC SUPPLIES & TECHNOLOGY, INC.·59 products·🇺🇸 United States

Catachem

FDA registration

CATACHEM, INC.·3 products·🇺🇸 United States

cobas INTEGRA D-DIMER

FDA registration

ROCHE DIAGNOSTICS GMBH·1 product·🇩🇪 Germany

REPROCESSED AUTOSUTURE UNIPOLAR LAPAROSCOPIC/ENDOSCOPIC INSTRUMENTS

FDA 510(k)

FDA Class 2 ·General, Plastic Surgery

ZYNERGY BALLOONPACE BALLOON GUIDED PACING AND MONITORING CATHETER

FDA 510(k)

FDA Class 2 ·Cardiovascular

Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

FDA classification

FDA Class 2 ·Electrosurgical, Cutting & Coagulation Accessories, Laparoscopic & Endoscopic, Reprocessed

Electrode, Pacemaker, Temporary

FDA classification

FDA Class 2 ·Electrode, Pacemaker, Temporary