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FDA 510(k)

Kisses Mini

K-Number: K170394 · 2017-10-06

ApplicantAchimhai Medical Corporation
Decision Date2017-10-06
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Kisses Mini is a medical device manufactured by Achimhai Medical Corporation. It received FDA 510(k) clearance on 2017-10-06 under approval number K170394. 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 Kisses Mini?

Kisses Mini is a medical device that received FDA 510(k) clearance on 2017-10-06. It is manufactured by Achimhai Medical Corporation. The 510(k) number is K170394.

When was Kisses Mini approved by the FDA?

Kisses Mini received FDA 510(k) clearance on 2017-10-06, under approval number K170394.

What company makes Kisses Mini?

Kisses Mini is manufactured by Achimhai Medical Corporation.

What is the FDA product code for Kisses Mini?

The FDA product code for Kisses Mini is DZE.

Other Devices by Achimhai Medical Corporation

K172630Kisses Plus Implant System K200193Kisses Plus Implant System

Related Devices (Code: DZE)

K160475Ritter Dental Implant SystemRitter Implants GmbH & Co. KG K161244s-Clean OneQ-SL Narrow Implant SystemDentis Co., Ltd. K163043Zeramex P6 Dental Implant SystemDentalpoint AG K161497Dental Implants and AbutmentsDitron Precision, Ltd. K153332ETIII SA Fixture System (O3.2mm)Hiossen, Inc. K151970KJ Mini Implant SystemKj Meditech 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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