Class Class II

ISO Abutment (K241183)

K241183 2025-07-28 Traditional
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Description

ISO Abutment by Seum Medi Co., Ltd., an FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241183
Clearance Date2025-07-28
Clearance TypeTraditional
Product CodeNHA
Regulation Number872.3630

Categories

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Predicate lineage for K241183

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. ISO Abutment (K241183) cites 12 predicate devices and is itself cited by 0 later devices.

Predicate devices cited by this clearance

Devices this clearance was compared against
K numberDeviceApplicantYear
K182615Surgikor Dental Implant SystemSurgikor, LLC2019
K181137IT-III active SystemNeobiotech Co., Ltd.2018
K161103US SA Implant SystemOsstem Implant Co., Ltd.2017
K160965SuperLineDentium Co., Ltd.2017
K160536Chaorum Implant SystemMedimecca Co., Ltd.2017
K161244s-Clean OneQ-SL Narrow Implant SystemDentis Co., Ltd.2016
K150938Straumann® Dental Implant System ¿ Roxolid® SLA ImplantsStraumann USA, LLC2015
K140091XPEED ANYRIDGE INTERNAL IMPLANT SYSYEMMegagen Implant Co., Ltd.2014
K121995TS FIXTURE SYSTEMOsstem Implant Co., Ltd.2012
K112787KERATORKj Meditech Co., Ltd.2012
K071638BIOHORIZONS TAPERED INTERNAL IMPLANT SYSTEMBioHorizons Implant Systems, Inc.2007
K0633413I OSSEOTITE CERTAIN DENTAL IMPLANTSImplant Innovations, Inc.2007

Trace the full predicate network for K241183

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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