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FDA 510(k)

IS-III active Short Implant

K-Number: K232049 · 2024-03-28

ApplicantNeobiotech Co., Ltd.
Decision Date2024-03-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IS-III active Short Implant is a medical device manufactured by Neobiotech Co., Ltd.. It received FDA 510(k) clearance on 2024-03-28 under approval number K232049. 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 IS-III active Short Implant?

IS-III active Short Implant is a medical device that received FDA 510(k) clearance on 2024-03-28. It is manufactured by Neobiotech Co., Ltd.. The 510(k) number is K232049.

When was IS-III active Short Implant approved by the FDA?

IS-III active Short Implant received FDA 510(k) clearance on 2024-03-28, under approval number K232049.

What company makes IS-III active Short Implant?

IS-III active Short Implant is manufactured by Neobiotech Co., Ltd..

What is the FDA product code for IS-III active Short Implant?

The FDA product code for IS-III active Short Implant is DZE.

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Other Devices by Neobiotech Co., Ltd.

K160991Neo GBR System K181137IT-III active System K181138IS-III active System K181178S-mini active Fixture K173938IS-III HActive Fixture K190849IS-III active System_S-narrow Type

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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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