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)

VIX WIN PRO

K-Number: K060178 · 2006-03-10

ApplicantGendex Dental Systems
Decision Date2006-03-10
Product CodeMUH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

VIX WIN PRO is the device name listed in this FDA 510(k) record. The listed applicant is Gendex Dental Systems. It received FDA 510(k) clearance on 2006-03-10 under 510(k) number K060178. The device is classified under product code MUH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VIX WIN PRO?

VIX WIN PRO is a medical device that received FDA 510(k) clearance on 2006-03-10. The listed applicant is Gendex Dental Systems. The 510(k) number is K060178.

When did VIX WIN PRO receive FDA 510(k) clearance?

VIX WIN PRO received FDA 510(k) clearance on 2006-03-10, under 510(k) number K060178.

Who is the listed applicant for VIX WIN PRO?

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

What is the FDA product code for VIX WIN PRO?

The FDA product code for VIX WIN PRO is MUH.

Other records listing Gendex Dental Systems 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.

K050255ARTHORALIX 8500, MODELS 110-0199G1, 110-0199G2, 110-0199G3, 110-0199G4

Related Devices (Code: MUH)

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.

K251793SOTA Cloud Smart Sensor (1.5)Sota Cloud Corp.K252570EzSensor HD, EzSensor UHDQpix Solutions, Inc.K250687Cocoon Solo (DX-7020s)Dexcowin Global, Inc.K251206Digital X-Ray DentiMax Pro Imaging SystemDentimax, Inc.K240040VistaPano S Ceph 2.0 (VistaPano S Ceph); VistaPano S 2.0 (VistaPano S); ProVecta S-Pan Ceph 2.0 (ProVecta S-Pan Ceph); ProVecta S-Pan 2.0 (ProVecta S-Pan)VATECH Co., Ltd.K242778X Sensor (Model: IOS-A15IF, HDI-15DGF)Qpix Solutions, 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.

↑