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FDA 510(k)

Valiant Curing Light

K-Number: K170101 · 2017-06-08

Decision Date2017-06-08
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Valiant Curing Light is the device name listed in this FDA 510(k) record. The listed applicant is Inter-Med/Vista Dental Products. It received FDA 510(k) clearance on 2017-06-08 under 510(k) number K170101. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Valiant Curing Light?

Valiant Curing Light is a medical device that received FDA 510(k) clearance on 2017-06-08. The listed applicant is Inter-Med/Vista Dental Products. The 510(k) number is K170101.

When did Valiant Curing Light receive FDA 510(k) clearance?

Valiant Curing Light received FDA 510(k) clearance on 2017-06-08, under 510(k) number K170101.

Who is the listed applicant for Valiant Curing Light?

The FDA 510(k) record lists Inter-Med/Vista Dental Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Valiant Curing Light?

The FDA product code for Valiant Curing Light is EBZ.

Other records listing Inter-Med/Vista Dental Products as applicant

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.

Related Devices (Code: EBZ)

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.

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.