Shantou Institute Of Ultrasonic Instruments Co., Ltd. (Siui)

FDA Regulatory Profile

Shantou Institute Of Ultrasonic Instruments Co., Ltd. (Siui) has 0 FDA recalls, 0 inspections, 8 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Aug 19, 2021

Updated: recalls Oct 23, 2026 · inspections Oct 23, 2026 · compliance actions Oct 23, 2026.

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Summary

Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K210317Apogee 1000/ Apogee 1000Neo/ Apogee 1000Lite/ Apogee 1000Exp/ Apogee 1000B/W / Apogee 1U/ Apogee 1T/…Aug 19, 2021
K210318Apogee 6500,Apogee 6300,Apogee 6200 Digital Color Doppler Ultrasound Imaging SystemAug 18, 2021
K202350SR-1000 Portable DR Imaging System, SR-1000S Portable DR Imaging SystemJan 6, 2021
K202353SR-2300 Portable DR Imaging System, SR-2300S Portable DR Imaging SystemDec 23, 2020
K200637SR-8100 Portable X-ray UnitJul 9, 2020
K200976SR-8230, SR-8230S Portable X-ray UnitJun 10, 2020
K173000Apogee 2100 Digital Color Doppler Ultrasound Imaging System Apogee 2300 Digital Color Doppler…Dec 7, 2017
K160853Apogee 5500/Apogee 5300/ Apogee 5800 Digital Color Doppler Ultrasound Imaging SystemJun 27, 2016