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FDA 510(k)

LIJIA Night Guard

K-Number: K241369 · 2024-08-22

ApplicantLijia, LLC
Decision Date2024-08-22
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

LIJIA Night Guard is a medical device manufactured by Lijia, LLC. It received FDA 510(k) clearance on 2024-08-22 under approval number K241369. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIJIA Night Guard?

LIJIA Night Guard is a medical device that received FDA 510(k) clearance on 2024-08-22. It is manufactured by Lijia, LLC. The 510(k) number is K241369.

When was LIJIA Night Guard approved by the FDA?

LIJIA Night Guard received FDA 510(k) clearance on 2024-08-22, under approval number K241369.

What company makes LIJIA Night Guard?

LIJIA Night Guard is manufactured by Lijia, LLC.

What is the FDA product code for LIJIA Night Guard?

The FDA product code for LIJIA Night Guard is MQC.

Related Clinical Trials

NCT07548502 Effect of Night Guard Use on Masseter Muscle Thickness in Children With Bruxism RECRUITING

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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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