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FDA 510(k)

DSG RELAXER SPLINT

K-Number: K022627 · 2003-03-18

ApplicantSentage Corporation D/B/A/ Dental Services Group
Decision Date2003-03-18
Product CodeMQC
DecisionSubstantially Equivalent

Device Summary

DSG RELAXER SPLINT is the device name listed in this FDA 510(k) record. The listed applicant is Sentage Corporation D/B/A/ Dental Services Group. It received FDA 510(k) clearance on 2003-03-18 under 510(k) number K022627. The device is classified under product code MQC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DSG RELAXER SPLINT?

DSG RELAXER SPLINT is a medical device that received FDA 510(k) clearance on 2003-03-18. The listed applicant is Sentage Corporation D/B/A/ Dental Services Group. The 510(k) number is K022627.

When did DSG RELAXER SPLINT receive FDA 510(k) clearance?

DSG RELAXER SPLINT received FDA 510(k) clearance on 2003-03-18, under 510(k) number K022627.

Who is the listed applicant for DSG RELAXER SPLINT?

The FDA 510(k) record lists Sentage Corporation D/B/A/ Dental Services Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DSG RELAXER SPLINT?

The FDA product code for DSG RELAXER SPLINT is MQC.

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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

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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