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FDA 510(k)

STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS

K-Number: K092951 · 2009-12-07

Decision Date2009-12-07
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS is the device name listed in this FDA 510(k) record. The listed applicant is Mectron S.P.A.. It received FDA 510(k) clearance on 2009-12-07 under 510(k) number K092951. 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 STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS?

STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS is a medical device that received FDA 510(k) clearance on 2009-12-07. The listed applicant is Mectron S.P.A.. The 510(k) number is K092951.

When did STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS receive FDA 510(k) clearance?

STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS received FDA 510(k) clearance on 2009-12-07, under 510(k) number K092951.

Who is the listed applicant for STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS?

The FDA 510(k) record lists Mectron S.P.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS?

The FDA product code for STARLIGHT PRO AND SILIVERLIGHT DENTAL CURING LIGHTS is EBZ.

Related Clinical Trials

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.

Other records listing Mectron S.P.A. 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.

View all 10 devices →

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.

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