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FDA 510(k)

JDEvolution Plus L and JDEvolution Plus LE

K-Number: K251148 · 2025-09-25

Decision Date2025-09-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

JDEvolution Plus L and JDEvolution Plus LE is the device name listed in this FDA 510(k) record. The listed applicant is Jdentalcare Srl. It received FDA 510(k) clearance on 2025-09-25 under 510(k) number K251148. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JDEvolution Plus L and JDEvolution Plus LE?

JDEvolution Plus L and JDEvolution Plus LE is a medical device that received FDA 510(k) clearance on 2025-09-25. The listed applicant is Jdentalcare Srl. The 510(k) number is K251148.

When did JDEvolution Plus L and JDEvolution Plus LE receive FDA 510(k) clearance?

JDEvolution Plus L and JDEvolution Plus LE received FDA 510(k) clearance on 2025-09-25, under 510(k) number K251148.

Who is the listed applicant for JDEvolution Plus L and JDEvolution Plus LE?

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

What is the FDA product code for JDEvolution Plus L and JDEvolution Plus LE?

The FDA product code for JDEvolution Plus L and JDEvolution Plus LE is DZE.

Other records listing Jdentalcare Srl 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.

Related Devices (Code: DZE)

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

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