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Shenzhen Future Electronic Co.,ltd: FDA-registered device maker in SHENZHEN Guangdong, China, 3 510(k) clearances

Name: Shenzhen Future Electronic Co.,ltd FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Shenzhen Future Electronic Co.,ltd is registered with the FDA (registration 3014344342) in SHENZHEN Guangdong, China. It lists 6 device types. The FDA files 3 510(k) clearances under its listings, the newest dated November 13, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3014344342
Address: Room 301,Building 1,Huahan Technology Industrial Park,No.16 Jinniu West Road,Heping Community,Pingshan, SHENZHEN Guangdong, China, 518116
Owner or operator: SHENZHEN FUTURE ELECTRONIC CO.,LTD (10057185)
Roles: Exporter to the US, Manufacturer
First device listed: March 5, 2018
Registered through: 2026
Brand names listed: Air Compression Therapy Device model: R-F003, Air Compression Therapy Device model: RP-ALM076H, Air Compression Therapy Device model: ST-501, Air Compression Therapy Device model: ST-502, Air Compression Therapy Device model: ST-503, Air Compression Therapy Device model: ST-504, Air Compression Therapy Device model: ST-505, Air Compression Therapy Device model: ST-506 and more

Devices it lists

Device	Product code	Class	Role	Source
Massager, Powered Inflatable Tube	IRP	2	Exporter to the US, Manufacturer	accessdata.fda.gov
Massager, Therapeutic, Electric	ISA	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Pad, Heating, Powered	IRT	2	Exporter to the US, Manufacturer	accessdata.fda.gov
Stimulator, Nerve, Transcutaneous, Over-The-Counter	NUH	2	Exporter to the US, Manufacturer	accessdata.fda.gov
Unit, Oral Irrigation	EFS	1	Exporter to the US, Manufacturer	accessdata.fda.gov
Vibrator, Therapeutic	IRO	1	Exporter to the US, 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
November 13, 2025	K251662	Air Compression Therapy Device (ST-504); Air Compression Therapy Device (ST-505); Air Compression Therapy Device (ST-506); Air Compression Therapy Device (ST-507)	IRP	Substantially Equivalent	Shenzhen Future Electronic Co., Ltd.	accessdata.fda.gov
September 13, 2022	K221092	Transcutaneous Electrical Nerve Stimulator Model: ST-304	NUH	Substantially Equivalent	Shenzhen Future Electronic Co., Ltd.	accessdata.fda.gov
March 31, 2022	K213745	Air Compression Therapy Device, model: ST-502	IRP	Substantially Equivalent	Shenzhen Future Electronic Co., Ltd.	accessdata.fda.gov

Compare with other makers

Updated November 13, 2025. 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.