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FDA 510(k)

DENTAL PROTECTOR

K-Number: K024261 · 2003-03-26

ApplicantDental Concepts, LLC
Decision Date2003-03-26
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

DENTAL PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Dental Concepts, LLC. It received FDA 510(k) clearance on 2003-03-26 under 510(k) number K024261. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DENTAL PROTECTOR?

DENTAL PROTECTOR is a medical device that received FDA 510(k) clearance on 2003-03-26. The listed applicant is Dental Concepts, LLC. The 510(k) number is K024261.

When did DENTAL PROTECTOR receive FDA 510(k) clearance?

DENTAL PROTECTOR received FDA 510(k) clearance on 2003-03-26, under 510(k) number K024261.

Who is the listed applicant for DENTAL PROTECTOR?

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

What is the FDA product code for DENTAL PROTECTOR?

The FDA product code for DENTAL PROTECTOR is MQC.

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Other records listing Dental Concepts, LLC 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.

K053580DOCTOR'S NIGHTGUARDK844238ORAPIK PERIODONTAL SCALER

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 NightGuardRemviaK251252NOBILCAM IMPAK DiscShandong Huge Dental Material CorporationK241729Hard Splint & Thermo-Adaptive SplintWhip Mix CorporationK243516Remi Custom Night GuardGrindguard, Inc.K241369LIJIA Night GuardLijia, LLC

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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