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Triowave Technologies

US

Last updated May 31, 2026

What Triowave Technologies makes

Triowave Technologies manufactures an analgesic transcutaneous electrical nerve stimulation (TENS) system marketed under the name PainKARE.

The TENS device is classified as Class II and is listed in the FDA 510(k) and FDA UDI registries; the company is based in the United States.

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

Information

Country
US
Address
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Website
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LinkedIn
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Facebook
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Email
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Phone
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PRRC Contact
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EUDAMED SRN
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FDA FEI Number
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DUNS Number
080195601

Catalogue (2)

DeviceModel / ReferenceRegistriesClassStatus
PainKARE PK001
FDA UDI
Class IIActive
PainKARE K151034
FDA 510(k)
Class IIActive

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