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FDA 510(k)

Overjet Charting Assist

K-Number: K233590 · 2024-02-23

ApplicantOverjet, Inc.
Decision Date2024-02-23
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Overjet Charting Assist is the device name listed in this FDA 510(k) record. The listed applicant is Overjet, Inc.. It received FDA 510(k) clearance on 2024-02-23 under 510(k) number K233590. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Overjet Charting Assist?

Overjet Charting Assist is a medical device that received FDA 510(k) clearance on 2024-02-23. The listed applicant is Overjet, Inc.. The 510(k) number is K233590.

When did Overjet Charting Assist receive FDA 510(k) clearance?

Overjet Charting Assist received FDA 510(k) clearance on 2024-02-23, under 510(k) number K233590.

Who is the listed applicant for Overjet Charting Assist?

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

What is the FDA product code for Overjet Charting Assist?

The FDA product code for Overjet Charting Assist is QIH.

Other records listing Overjet, Inc. 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.

View all 12 devices →

Related Devices (Code: QIH)

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.

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.