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FDA 510(k)

DAND Dental Implant System

K-Number: K250176 · 2025-04-21

Decision Date2025-04-21
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DAND Dental Implant System is the device name listed in this FDA 510(k) record. The listed applicant is D.A.N.D. Metal Industries North, Ltd.. It received FDA 510(k) clearance on 2025-04-21 under 510(k) number K250176. 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 DAND Dental Implant System?

DAND Dental Implant System is a medical device that received FDA 510(k) clearance on 2025-04-21. The listed applicant is D.A.N.D. Metal Industries North, Ltd.. The 510(k) number is K250176.

When did DAND Dental Implant System receive FDA 510(k) clearance?

DAND Dental Implant System received FDA 510(k) clearance on 2025-04-21, under 510(k) number K250176.

Who is the listed applicant for DAND Dental Implant System?

The FDA 510(k) record lists D.A.N.D. Metal Industries North, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DAND Dental Implant System?

The FDA product code for DAND Dental Implant System is DZE.

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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