Class Class II
Klockner Abutments (K230103)
Description
Klockner Abutments by SOADCO, S.L., an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK230103
Clearance Date2023-04-24
Clearance TypeTraditional
Product CodeNHA
Regulation Number872.3630
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K230103
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. Klockner Abutments (K230103) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K222288 | DESS Dental Smart Solutions | Terrats Medical SL | 2022 |
| K220612 | PrimeLOC Attachment System | Innovative Product Brands, Inc. | 2022 |
| K191123 | Multi-unit Abutments | Medentika GmbH | 2020 |
| K170022 | Klockner Vega TiBase for CEREC | SOADCO, S.L. | 2017 |
| K151194 | KLOCKNER DENTAL IMPLANT ABUTMENTS (II) | SOADCO, S.L. | 2016 |
Trace the full predicate network for K230103
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.