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FDA 510(k)

Adin Customized Abutments

K-Number: K250178 · 2025-10-17

Decision Date2025-10-17
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Adin Customized Abutments is the device name listed in this FDA 510(k) record. The listed applicant is Adin Dental Implant Systems , Ltd.. It received FDA 510(k) clearance on 2025-10-17 under 510(k) number K250178. 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 Adin Customized Abutments?

Adin Customized Abutments is a medical device that received FDA 510(k) clearance on 2025-10-17. The listed applicant is Adin Dental Implant Systems , Ltd.. The 510(k) number is K250178.

When did Adin Customized Abutments receive FDA 510(k) clearance?

Adin Customized Abutments received FDA 510(k) clearance on 2025-10-17, under 510(k) number K250178.

Who is the listed applicant for Adin Customized Abutments?

The FDA 510(k) record lists Adin Dental Implant Systems , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Adin Customized Abutments?

The FDA product code for Adin Customized Abutments is NHA.

Other records listing Adin Dental Implant Systems , Ltd. 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: 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

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