ARCHITEX

FDA registration

MEDTRONIC SOFAMOR DANEK USA, INC.·2 products·🇺🇸 United States

ARCHITEX

FDA registration

WARSAW ORTHOPEDIC, INC.·2 products·🇺🇸 United States

ARCHITEX

FDA registration

Medtronic Engineering and Innovation Center (MEIC)·2 products·🇮🇳 India

ARCHITEX SPACE MAINTENANCE SYSTEM

FDA 510(k)

FDA Class 2 ·Dental

Vonco Products, LLC

FDA registration

Vonco Products, LLC·1 product·🇺🇸 United States

FORA

FDA registration

FORA CARE INC.·1 product·🇺🇸 United States

ActiveCare+SFT System

FDA registration

ZIMMER SURGICAL, INC.·1 product·🇺🇸 United States

Vital Signs Monitor

FDA registration

TAIDOC TECHNOLOGY CORPORATION·1 product·🇹🇼 Taiwan

Utrecht Interstitial Fletcher CT/MR Applicator

FDA UDI

Nucletron B.V.·08717213034778·Interstitial Ovoid (left) 20mm 25°, R10

Plate, Bone

FDA classification

FDA Class 2 ·Plate, Bone

UniTip High Resolution Catheter

FDA UDI

Unisensor AG·07640172971178·

UniTip High Resolution Catheter

FDA UDI

Unisensor AG·07640172972991·

UniTip High Resolution Catheter

FDA UDI

Unisensor AG·07640172973271·

MEDIFACE PACS

FDA 510(k)

FDA Class 2 ·Radiology

V-TRUST TD-8002 MULTI-PARAMETER SPOT-CHECK MONITOR MODEL TD-8002

FDA 510(k)

FDA Class 2 ·Cardiovascular

Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

FDA classification

FDA Class 2 ·Monitor, Physiological, Patient (Without Arrhythmia Detection Or Alarms)

System, Image Processing, Radiological

FDA classification

FDA Class 2 ·System, Image Processing, Radiological