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Shenzhen Kingyield Technology Co., Ltd: FDA-registered device maker in Shen Zhen Guangdong, China, 5 510(k) clearances

Name: Shenzhen Kingyield Technology Co., Ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shenzhen Kingyield Technology Co., Ltd is registered with the FDA (registration 3007420856) in Shen Zhen Guangdong, China. It lists 3 device types. The FDA files 5 510(k) clearances under its listings, the newest dated October 6, 2018. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number: 3007420856
Address: No. 301, Bldg 1, Cuigang Industrail Zone 3, Huaide Community FuYong street, Baoan District, Shen Zhen Guangdong, China, 518103
Owner or operator: SHENZHEN KINGYIELD TECHNOLOGY CO., LTD (10027808)
Roles: Manufacturer
First device listed: December 4, 2008
Registered through: 2027
Brand names listed: Noninvasive Blood Pressure Measurement System, NuvoMed/BP101K, NuvoMed/BP310B, OximeterSleepOSR1, OximeterSleepRingOSR2, OximeterSleepRingOSR3, SleepOximeterRingSOR1, SleepOximeterRingSOR1, SleepOximeterRingSOR2, SleepOximeterSOR3, SmartRingSR1, SmartRingSR2, SmartRingSR3,SmartRingOximeterSRO1, SmartRingOximeterSRO2, SmartRingSRO3, SmartRingOximeterSleepSROS1, SmartRingOximeterSROS2, SmartRingOximeterSleepSROS3

Devices it lists

Device	Product code	Class	Role	Source
Oximeter	DQA	2	Manufacturer	accessdata.fda.gov
Oximeter, Wellness	PGJ	2	Manufacturer	accessdata.fda.gov
System, Measurement, Blood-Pressure, Non-Invasive	DXN	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
October 6, 2018	K182018	Bluetooth blood pressure monitor	DXN	Substantially Equivalent	Shenzhen Kingyield Technology Co., Ltd.	accessdata.fda.gov
May 28, 2013	K123801	FINGER PULSE OXIMETER	DQA	Substantially Equivalent	Shenzhen Kingyield Technology Co., Ltd.	accessdata.fda.gov
February 10, 2012	K112042	KINGYIELD WRIST BLOOD PRESSURE MONITOR	DXN	Substantially Equivalent	Shenzhen Kingyield Technology Co., Ltd.	accessdata.fda.gov
October 27, 2008	K083043	KING`YIELD WRIST BLOOD PRESSURE MONITOR, MODEL BP201	DXN	Substantially Equivalent	Shenzhen Kingyield Technology Co., Ltd.	accessdata.fda.gov
March 23, 2007	K062033	BP 101 DIGITAL BLOOD PRESSURE MONITOR	DXN	Substantially Equivalent	Kingyield Hongkong Limited	accessdata.fda.gov

Compare with other makers

Updated October 6, 2018. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.