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)

Visionbody

K-Number: K222386 · 2023-02-24

ApplicantVb Technologies AG
Decision Date2023-02-24
Product CodeNGX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

Visionbody is a medical device manufactured by Vb Technologies AG. It received FDA 510(k) clearance on 2023-02-24 under approval number K222386. The device is classified under product code NGX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Visionbody?

Visionbody is a medical device that received FDA 510(k) clearance on 2023-02-24. It is manufactured by Vb Technologies AG. The 510(k) number is K222386.

When was Visionbody approved by the FDA?

Visionbody received FDA 510(k) clearance on 2023-02-24, under approval number K222386.

What company makes Visionbody?

Visionbody is manufactured by Vb Technologies AG.

What is the FDA product code for Visionbody?

The FDA product code for Visionbody is NGX.

Related Devices (Code: NGX)

K152420AK Body Toning DeviceAk Beauty Enterprises, LLC K161974SLENDERTONE® Connect Abs, Type 570Bio-Medical Research, Ltd. K152480Revitive Medic; Revitive MV; Revitive LVActegy , Ltd. K151722Slim UP ULTRAAime Medical, Inc. K172876PowerDot PD-01MSmartmissimo Technologies Pte, Ltd. K172241Tyece OTC EMS System, Model EM35Tyece , Ltd.

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.

↑