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FDA 510(k)

Trinity ELE Plus and Trinity ELE Plus Pro

K-Number: K201906 · 2021-02-24

ApplicantCarol Cole Company Dba Nuface
Decision Date2021-02-24
Product CodeNFO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Trinity ELE Plus and Trinity ELE Plus Pro is a medical device manufactured by Carol Cole Company Dba Nuface. It received FDA 510(k) clearance on 2021-02-24 under approval number K201906. The device is classified under product code NFO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Trinity ELE Plus and Trinity ELE Plus Pro?

Trinity ELE Plus and Trinity ELE Plus Pro is a medical device that received FDA 510(k) clearance on 2021-02-24. It is manufactured by Carol Cole Company Dba Nuface. The 510(k) number is K201906.

When was Trinity ELE Plus and Trinity ELE Plus Pro approved by the FDA?

Trinity ELE Plus and Trinity ELE Plus Pro received FDA 510(k) clearance on 2021-02-24, under approval number K201906.

What company makes Trinity ELE Plus and Trinity ELE Plus Pro?

Trinity ELE Plus and Trinity ELE Plus Pro is manufactured by Carol Cole Company Dba Nuface.

What is the FDA product code for Trinity ELE Plus and Trinity ELE Plus Pro?

The FDA product code for Trinity ELE Plus and Trinity ELE Plus Pro is NFO.

Other Devices by Carol Cole Company Dba Nuface

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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