Jkh Health Co., Ltd. is one of 1554 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Jkh Health Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Cryon-X Cold Compression, Ultrasound Stimulator, Cold Compression
10
Total
10
Cleared
0
Denied
Jkh Health Co., Ltd. has 10 FDA 510(k) cleared medical devices. Based in Shenzhen, CN.
Latest FDA clearance: Oct 2025. Active since 2016. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Jkh Health Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Jkh USA, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Jkh Health Co., Ltd.
10 devices
Cleared
Oct 24, 2025
Cryon-X Cold Compression
Physical Medicine
29d
Cleared
Jun 04, 2025
Ultrasound Stimulator
Physical Medicine
439d
Cleared
May 01, 2024
Cold Compression
Physical Medicine
21d
Cleared
Feb 23, 2024
Lymphedema Compression
Cardiovascular
52d
Cleared
Oct 27, 2023
Cold/Hot Compression
Physical Medicine
336d
Cleared
Nov 28, 2022
Infrared Thermometer, Model: JKH-300, JKH-301, JKH-302, JKH-303, JKH-304
General Hospital
599d
Cleared
Jan 21, 2021
Overlapped Compression Therapy
Cardiovascular
118d
Cleared
Jul 01, 2020
StimPlus Patch, StimPlus Patch, StimPlus Patch
Neurology
119d
Cleared
Apr 14, 2017
Electronic Pulse Stimulator Model: PL-029K12 and PL-029K13
Neurology
217d
Cleared
May 05, 2016
Electronic Pulse Stimulator
Neurology
149d