Motive™ Muscle Stimulator for Lower Back (OT01-1003)

FDA 510(k) K253478 · Motive Health, Inc.

Substantially Equivalent

510(k) numberK253478

Submission

Device name
Motive™ Muscle Stimulator for Lower Back (OT01-1003)
Applicant
Motive Health, Inc.
Tempe, AZ, US
Received
October 14, 2025
Decision date
November 6, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
NGX – Stimulator, Muscle, Powered, For Muscle Conditioning
Device class
Class II (moderate risk)
Regulation
21 CFR 890.5850
Specialty
Physical Medicine

A powered muscle stimulator for muscle conditioning is a device used for other than medical purposes to apply an electrical current to electrodes on a person's skin to temporarily affect the stimulated muscle's contractile properties, force output, and/or fatigue resistance. Unlike the classified Powered Muscle Stimulator devices intended for use in physical medicine and rehabilitation, this…

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K253790High Intensity Focused Electromagnetic Stimulation Device (FE60)NGX · Traditional Beijing Winkonlaser Technology Limited08/13/2026SE
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K253408CoolToneNGX · Traditional Zimmer Medizinsysteme GmbH01/16/2026SE
K252154Portable Electro Stimulation Therapy Device (LGT-2320BE, LGT-2320ME, and LGT-2320SP)NGX · Traditional Guangzhou Longest Medical Technology Co., Ltd.12/09/2025SE
K251594truFlexNGX · Special Syrma Johari Medtech Limited08/28/2025SE
K251706TENS and EMS UnitNGX · Special Changsha Anxiang Medical Technology Co., Ltd.07/30/2025SE
K251378CoolToneNGX · Special Zimmer Medizinsysteme GmbH07/14/2025SE
K251746Pure ImpactNGX · Special Sofwave Medical, Ltd.07/02/2025SE
K2507593 in 1 TENS UNITNGX · Traditional Changsha Anxiang Medical Technology Co., Ltd.06/13/2025SE

Questions and answers

When was Motive™ Muscle Stimulator for Lower Back (OT01-1003) cleared by the FDA?

Motive™ Muscle Stimulator for Lower Back (OT01-1003) (K253478) received a 510(k) decision of Substantially Equivalent on November 6, 2025, 23 days after the submission was received.

What is the product code of K253478?

The FDA product code is NGX – Stimulator, Muscle, Powered, For Muscle Conditioning, a Class II (moderate risk) device regulated under 21 CFR 890.5850.