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FDA 510(k)

INOSS System

K-Number: K260006 · 2026-06-17

ApplicantInosys, Inc.
Decision Date2026-06-17
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INOSS System is the device name listed in this FDA 510(k) record. The listed applicant is Inosys, Inc.. It received FDA 510(k) clearance on 2026-06-17 under 510(k) number K260006. 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 INOSS System?

INOSS System is a medical device that received FDA 510(k) clearance on 2026-06-17. The listed applicant is Inosys, Inc.. The 510(k) number is K260006.

When did INOSS System receive FDA 510(k) clearance?

INOSS System received FDA 510(k) clearance on 2026-06-17, under 510(k) number K260006.

Who is the listed applicant for INOSS System?

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

What is the FDA product code for INOSS System?

The FDA product code for INOSS 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.

K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K252731Promimic ZrP Surface Dental Implant; Promimic ZrP + HAnano Surface Dental ImplantPromimic ABK252031Adin Long Dental Implant SystemAdin Dental Implant Systems , Ltd.K253334ZENEX Implant System_Short (R-System)Izenimplant Co., Ltd.

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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