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FDA 510(k)

Dental diode laser

K-Number: K214008 · 2022-05-10

ApplicantShenzhen Soga Technology Co., Ltd.
Decision Date2022-05-10
Product CodeNVK
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Dental diode laser is a medical device manufactured by Shenzhen Soga Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-05-10 under approval number K214008. The device is classified under product code NVK. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Dental diode laser?

Dental diode laser is a medical device that received FDA 510(k) clearance on 2022-05-10. It is manufactured by Shenzhen Soga Technology Co., Ltd.. The 510(k) number is K214008.

When was Dental diode laser approved by the FDA?

Dental diode laser received FDA 510(k) clearance on 2022-05-10, under approval number K214008.

What company makes Dental diode laser?

Dental diode laser is manufactured by Shenzhen Soga Technology Co., Ltd..

What is the FDA product code for Dental diode laser?

The FDA product code for Dental diode laser is NVK.

Related Clinical Trials

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Other Devices by Shenzhen Soga Technology Co., Ltd.

K211150Dental diode laser, SOGA Laser, ILaser II

Related Devices (Code: NVK)

K213428EdgeProBiolase, Inc. K210350Gemini 2 810+980 Soft Tissue LaserAzena Medical, LLC K203396DEKA SMARTPERIOEl.En Electronic Engineering Spa K201387Ultrafast, Ultrafast Plus, Ultrafast LiteDentlight, Inc. K221761SoleaConvergent Dental, Inc. K211150Dental diode laser, SOGA Laser, ILaser IIShenzhen Soga Technology Co., Ltd.

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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