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

FDA 510(k)

CloudPoint FastDesign Chairside

K-Number: K231529 · 2024-03-14

Decision Date2024-03-14
Product CodePNP
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CloudPoint FastDesign Chairside is the device name listed in this FDA 510(k) record. The listed applicant is Prismatik Dentalcraft, Inc.. It received FDA 510(k) clearance on 2024-03-14 under 510(k) number K231529. The device is classified under product code PNP. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CloudPoint FastDesign Chairside?

CloudPoint FastDesign Chairside is a medical device that received FDA 510(k) clearance on 2024-03-14. The listed applicant is Prismatik Dentalcraft, Inc.. The 510(k) number is K231529.

When did CloudPoint FastDesign Chairside receive FDA 510(k) clearance?

CloudPoint FastDesign Chairside received FDA 510(k) clearance on 2024-03-14, under 510(k) number K231529.

Who is the listed applicant for CloudPoint FastDesign Chairside?

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

What is the FDA product code for CloudPoint FastDesign Chairside?

The FDA product code for CloudPoint FastDesign Chairside is PNP.

Other records listing Prismatik Dentalcraft, 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 36 devices →

Related Devices (Code: PNP)

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.