Synergy Health Daniken AG

FDA registration

Synergy Health Daniken AG·1 product·🇨🇭 Switzerland

RUETSCHI TECHNOLOGY AG

FDA registration

RUETSCHI TECHNOLOGY AG·1 product·🇨🇭 Switzerland

M6-C™ Single Use, Disposable Instrumentation

FDA 510(k)

FDA Class 2 ·Orthopedic

Manual Instruments Designed For Use With Total Disc Replacement Devices

FDA classification

FDA Class 2 ·Manual Instruments Designed For Use With Total Disc Replacement Devices

DePuy Mitek, Inc.

FDA registration

DePuy Mitek, Inc.·1 product·🇺🇸 United States

PANALOK RC QUICKANCHOR PLUS, MODEL 212130, 212730; DUAL SUTURE PANALOK RC QUICKANCHOR PLLUS, MODELS 212132, 212732

FDA registration

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

EZ-IO INTRAOSSEOUS INFUSION SYSTEM

FDA registration

Arrow International, LLC (subsidiary of Teleflex Incorporated)·1 product·🇺🇸 United States

EZ-IO

FDA registration

Teleflex Medical LLC·1 product·🇺🇸 United States

INNOVATIVE MEDICAL MANUFACTURING CO.

FDA registration

INNOVATIVE MEDICAL MANUFACTURING CO.·1 product·🇹🇼 Taiwan

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

Hough™ COVID-19 Antigen Home Test

FDA registration

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

EZ-IO INTRAOSSEOUS INFUSION SYSTEM

FDA 510(k)

FDA Class 2 ·General Hospital

PANALOK RC QUICKANCHOR PLUS, MODEL 212130, 212730; DUAL SUTURE PANALOK RC QUICKANCHOR PLLUS, MODELS 212132, 212732

FDA 510(k)

FDA Class 2 ·Orthopedic

Staple, Fixation, Bone

FDA classification

FDA Class 2 ·Staple, Fixation, Bone

Needle, Hypodermic, Single Lumen

FDA classification

FDA Class 2 ·Needle, Hypodermic, Single Lumen