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FDA 510(k)

PreXolid CAD/CAM abutments

K-Number: K240725 · 2024-10-18

ApplicantEclectic Co., Ltd.
Decision Date2024-10-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PreXolid CAD/CAM abutments is a medical device manufactured by Eclectic Co., Ltd.. It received FDA 510(k) clearance on 2024-10-18 under approval number K240725. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PreXolid CAD/CAM abutments?

PreXolid CAD/CAM abutments is a medical device that received FDA 510(k) clearance on 2024-10-18. It is manufactured by Eclectic Co., Ltd.. The 510(k) number is K240725.

When was PreXolid CAD/CAM abutments approved by the FDA?

PreXolid CAD/CAM abutments received FDA 510(k) clearance on 2024-10-18, under approval number K240725.

What company makes PreXolid CAD/CAM abutments?

PreXolid CAD/CAM abutments is manufactured by Eclectic Co., Ltd..

What is the FDA product code for PreXolid CAD/CAM abutments?

The FDA product code for PreXolid CAD/CAM abutments is NHA.

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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.

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