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SME, INC. USA

US

Last updated May 30, 2026

What SME, INC. USA makes

SME, Inc. manufactures single-use transcutaneous electrical stimulation (TENS) electrodes and skin topical coupling gels designed for temporary adhesion and electrical conductivity during neuromuscular stimulation therapies. These products are intended for use with external electrical stimulation devices to deliver therapeutic currents to the skin.

The company’s portfolio is classified under Class II devices in the US and is listed in the FDA’s Unique Device Identifier (UDI) database. The products are regulated under the jurisdiction of the US Food and Drug Administration.

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

Information

Country
US
Address
—
Website
smeincusa.com
LinkedIn
—
Facebook
—
Phone
910-798-0500
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
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DUNS Number
008264868

Catalogue (14)

DeviceModel / ReferenceRegistriesClassStatus
Sme W116
FDA UDI
Class IIActive
Sme SMEG
FDA UDI
Class IIActive
Sme F202
FDA UDI
Class IIActive
Sme SMEG
FDA UDI
Class IIUnknown
Sme F204
FDA UDI
Class IIActive
Sme W110
FDA UDI
Class IIActive
Sme W102
FDA UDI
Class IIActive
Sme W100
FDA UDI
Class IIActive
Sme W104
FDA UDI
Class IIActive
Sme F206
FDA UDI
Class IIActive
Sme F210
FDA UDI
Class IIActive
Sme SMEL
FDA UDI
Class IIUnknown
Sme W106
FDA UDI
Class IIActive
Sme SMEL
FDA UDI
Class IIActive

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