FDA 510(k)

X-View 3D Pan/X-View 2D Pan

K-Number: K222666 · 2023-07-10

Decision Date2023-07-10

Product CodeOAS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

X-View 3D Pan/X-View 2D Pan is a medical device manufactured by Trident S.R.L. It received FDA 510(k) clearance on 2023-07-10 under approval number K222666. The device is classified under product code OAS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the X-View 3D Pan/X-View 2D Pan?

X-View 3D Pan/X-View 2D Pan is a medical device that received FDA 510(k) clearance on 2023-07-10. It is manufactured by Trident S.R.L. The 510(k) number is K222666.

When was X-View 3D Pan/X-View 2D Pan approved by the FDA?

X-View 3D Pan/X-View 2D Pan received FDA 510(k) clearance on 2023-07-10, under approval number K222666.

What company makes X-View 3D Pan/X-View 2D Pan?

X-View 3D Pan/X-View 2D Pan is manufactured by Trident S.R.L.

What is the FDA product code for X-View 3D Pan/X-View 2D Pan?

The FDA product code for X-View 3D Pan/X-View 2D Pan is OAS.

Other Devices by Trident S.R.L

K162619I View and Imagen Sensor K160386ReadeR, VieweR, QuickScan PSP K182206RiX70 DC K200625I-View Gold and Imagen Gold Dental Sensors

Related Devices (Code: OAS)

K161900HYPERION X5Cefla S.C. K160166X-MIND triumDe Gotzen S.R.L. K162085i-CAT FLX V series / KaVo 3D eXam+ V seriesImaging Sciences International K160882PaX-i3D Green Premium (Model: PCT-90LH)VATECH Co., Ltd. K162660Green Smart (Model: PHT-35LHS)VATECH Co., Ltd. K161881PreXion3D ExcelsiorPrexion Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.