Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Videa Perio Assist

K-Number: K223296 · 2023-02-06

ApplicantVideahealth, Inc.
Decision Date2023-02-06
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Videa Perio Assist is a medical device manufactured by Videahealth, Inc.. It received FDA 510(k) clearance on 2023-02-06 under approval number K223296. 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 Videa Perio Assist?

Videa Perio Assist is a medical device that received FDA 510(k) clearance on 2023-02-06. It is manufactured by Videahealth, Inc.. The 510(k) number is K223296.

When was Videa Perio Assist approved by the FDA?

Videa Perio Assist received FDA 510(k) clearance on 2023-02-06, under approval number K223296.

What company makes Videa Perio Assist?

Videa Perio Assist is manufactured by Videahealth, Inc..

What is the FDA product code for Videa Perio Assist?

The FDA product code for Videa Perio Assist is QIH.

Other Devices by Videahealth, Inc.

K213795Videa Caries Assist K232384Videa Dental Assist K251002Videa Dental AI

Related Devices (Code: QIH)

K191647QLAB Advanced Quantification SoftwarePhilips Health Care K191171EchoGo CoreUltromics, Ltd. K201195syngo.via MI Workflows, syngo MBFSiemens Medical Solutions USA, Inc. K202013WRDensity by Whiterabbit.aiWhiterabbit.Ai, Inc. K202546LVivo SeamlessDia Imaging Analysis, Ltd. K193283AI-Rad Companion Prostate MRSiemens Medical Solutions USA, Inc.

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.

↑