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The Sun Co.

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Devices
1

What The Sun Co. makes

The Sun Co. manufactures the TRANS-PULSE Model #1103, a medical device designed for transcutaneous electrical nerve stimulation (TENS) therapy to manage pain.

The TRANS-PULSE Model #1103 is classified as a Class II device under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Trans-Pulse Model #1103 Ref K862355

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does The Sun Co. have in the registry?

The registry currently lists 1 device for The Sun Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Sun Co.'s devices?

Among its 1 most recently registered device, The Sun Co. has devices listed in FDA 510(k) (1 device).

What risk classes do The Sun Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for The Sun Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Sun Co. in the registry?

The most recently registered devices listed for The Sun Co. include TRANS-PULSE MODEL #1103.

Generated automatically from registry data and not verified by a human reviewer.