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Dynatronics Corp.

Last updated May 23, 2026

What Dynatronics Corp. makes

Dynatronics Corp. manufactures transcutaneous electrical stimulation electrodes and leads, multi-modality physical therapy systems, ultrasound system applicators and systems, intermittent powered traction systems, light-energy skin surface treatment system applicators, and skin topical coupling gels and lotions for professional-use physical therapy settings.

The company's devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) and FDA UDI registries; Dynatronics Corp. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of devices does Dynatronics Corp. manufacture?

Where is Dynatronics Corp. based?

Dynatronics Corp. is based in the United States, as stated in the company's country information provided in the device data.

In which regulatory registries are Dynatronics Corp.'s devices listed?

Dynatronics Corp.'s devices are listed in the FDA 510(k) and FDA UDI registries, as specified in the LISTED IN field of the device data.

How are Dynatronics Corp.'s devices classified?

Dynatronics Corp.'s devices are classified as Class I and Class II medical devices, according to the DEVICE CLASSES field in the provided data.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
Website: —
LinkedIn: —
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Email: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (130)

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Device	Model / Reference	Registries	Class	Status
Superior Foam Electrodes 2" Round	DSF2R-CS	FDA UDI	Class II	Unknown
DynaFlex (Foam) 2.75" Round	DF2.75RF	FDA UDI	Class II	Active
50 Plus Soundhead	CM10SH	FDA UDI	Class II	Unknown
50 Plus Soundhead	CM05SH	FDA UDI	Class II	Unknown
DynaFlex (Foam) 2" Round	DF2RF	FDA UDI	Class II	Active
Dynatron 400	K924319	FDA 510(k)	Class II	Active
Dynatron Tri-Wave Light Pad Dynatron Tri-Wave Light Probe	K113250	FDA 510(k)	Class II	Active
Dynatron 360 Range Of Motion Testing Device	K897178	FDA 510(k)	Class I	Active
Dynatron Sts	K010565	FDA 510(k)	Class II	Active
Dynatron 2000	K880912	FDA 510(k)	Class I	Active
Dynatron 950	K950349	FDA 510(k)	Class II	Active
Dynatron Ibox Iontophoresis Device	K043047	FDA 510(k)	Class II	Active
Dynatron Thermostim Probe-Done	K120835	FDA 510(k)	Class II	Active
Dynatron Dx2 Traction Unit	K051680	FDA 510(k)	Class II	Active
Dynatron 550	K941577	FDA 510(k)	Class II	Active
Dynatron Solaris Series, Models 705, 706, 708, 709 D880 Infrared Probe (optional Accessory)	K031329	FDA 510(k)	Class II	Active
Dynatron Peltier Thermostim Probe	K132057	FDA 510(k)	Class II	Active
Solaris D890 Therapy Probe	K040729	FDA 510(k)	Class II	Active
Dynatron 900	K993919	FDA 510(k)	Class II	Active
Dynatron Ion Iontophoresis Electrode	K060814	FDA 510(k)	Class II	Active
Dynatron 250	K944935	FDA 510(k)	Class II	Active
Dynatron X3 , Dynatron Xp Ir Light Pad, D405 Ir Light Probe	K051261	FDA 510(k)	Class II	Active
Dynatron 650	K950348	FDA 510(k)	Class II	Active
Dynatron 150	K935728	FDA 510(k)	Class II	Active
Dynatron 800	K932937	FDA 510(k)	Class II	Active
Dynatron 125 Ultrasound	K961250	FDA 510(k)	Class II	Active
Dynatron 500	K870947	FDA 510(k)	Class II	Active
Dynatron Sts Rx	K010948	FDA 510(k)	Class II	Active
Dynatron 200 Microcurrent	K903577	FDA 510(k)	Class II	Active
Dynatron 525	K961261	FDA 510(k)	Class II	Active

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