PreXolid CAD/CAM abutments
K-Number: K240725 · 2024-10-18
Device Summary
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. The listed applicant is Eclectic Co., Ltd.. The 510(k) number is K240725.
When did PreXolid CAD/CAM abutments receive FDA 510(k) clearance?
PreXolid CAD/CAM abutments received FDA 510(k) clearance on 2024-10-18, under 510(k) number K240725.
Who is the listed applicant for PreXolid CAD/CAM abutments?
The FDA 510(k) record lists Eclectic Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PreXolid CAD/CAM abutments?
The FDA product code for PreXolid CAD/CAM abutments is NHA.
Related Devices (Code: NHA)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.