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FDA 510(k)

Tria Sapphire

K-Number: K160821 · 2016-06-15

ApplicantTria Beauty, Inc.
Decision Date2016-06-15
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Tria Sapphire is the device name listed in this FDA 510(k) record. The listed applicant is Tria Beauty, Inc.. It received FDA 510(k) clearance on 2016-06-15 under 510(k) number K160821. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Tria Sapphire?

Tria Sapphire is a medical device that received FDA 510(k) clearance on 2016-06-15. The listed applicant is Tria Beauty, Inc.. The 510(k) number is K160821.

When did Tria Sapphire receive FDA 510(k) clearance?

Tria Sapphire received FDA 510(k) clearance on 2016-06-15, under 510(k) number K160821.

Who is the listed applicant for Tria Sapphire?

The FDA 510(k) record lists Tria Beauty, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Tria Sapphire?

The FDA product code for Tria Sapphire is OLP.

Related Devices (Code: OLP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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

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