Jkh USA, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Jkh USA, LLC - FDA 510(k) Cleared Devices
Recent clearances: PlusCare Temperature Probes, Skin Types: PT2252-AS, PTHP-AS, PTMQ-AS, PTSW-AS, PTSM-15AS, PTSL-AS, PTMR-AS, Patient Monitoring Cables, Blood Pressure Cuff, U1883S,U1883D, U1882S, U1882D, U1881S, U1881D, Blood Pressure Cuff, U1885S, U1885D, U1880S, U1880D, U1886S, U1886D, Blood Pressure Cuff, U1869S, U1869D, U1889S, U1889D, U1884S, U1884D, Blood Pressure Cuff, U1710S, U1720S, U1730S,U1740S, U1750S, U1760S, Blood Pressure Cuff, U1770S, U1790s, U1710D, U1720D, U1730D, U1740D
9
Total
9
Cleared
0
Denied
Jkh USA, LLC has 9 FDA 510(k) cleared medical devices. Based in Diamond Bar, US.
Last cleared in 2021. Active since 2019.
Browse the FDA 510(k) cleared devices submitted by Jkh USA, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Jkh USA, LLC
9 devices
Cleared
Aug 31, 2021
PlusCare Temperature Probes, Skin Types: PT2252-AS, PTHP-AS, PTMQ-AS,...
General Hospital
260d
Cleared
Feb 05, 2021
Patient Monitoring Cables
Cardiovascular
53d
Cleared
Jan 06, 2021
Blood Pressure Cuff, U1883S,U1883D, U1882S, U1882D, U1881S, U1881D, Blood...
Cardiovascular
23d
Cleared
Nov 27, 2020
Spo2 Sensor
Anesthesiology
60d
Cleared
Sep 15, 2020
Massage Compression Boots
Physical Medicine
90d
Cleared
Sep 08, 2020
Disposable Medical Face Mask
General Hospital
97d
Cleared
Sep 21, 2019
Medi-Direct TENS Pen
Neurology
360d
Cleared
Jun 21, 2019
JKH Stimulator Plus
Neurology
51d
Cleared
Mar 14, 2019
JKH Stimulator Plus
Neurology
211d