FDA 510(k)

LIJIA Night Guard

K-Number: K241369 · 2024-08-22

Decision Date2024-08-22

Product CodeMQC

DecisionSubstantially Equivalent

Device Summary

LIJIA Night Guard is the device name listed in this FDA 510(k) record. The listed applicant is Lijia, LLC. It received FDA 510(k) clearance on 2024-08-22 under 510(k) 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. The listed applicant is Lijia, LLC. The 510(k) number is K241369.

When did LIJIA Night Guard receive FDA 510(k) clearance?

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

Who is the listed applicant for LIJIA Night Guard?

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

What is the FDA product code for LIJIA Night Guard?

The FDA product code for LIJIA Night Guard is MQC.

Related Devices (Code: MQC)

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.

K253798UltraPrint-Dental Hard Splint UVGuangzhou Heygears IMC., Inc.K250743Remvia NightGuardRemvia K251252NOBILCAM IMPAK DiscShandong Huge Dental Material Corporation K241729Hard Splint & Thermo-Adaptive SplintWhip Mix Corporation K243516Remi Custom Night GuardGrindguard, Inc.K231775GR Resin System MSIPro3Dure Medical

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.