Medentika CAD/CAM Abutments (K242542)
Description
Medentika CAD/CAM Abutments by Medentika GmbH, an FDA 510(k) cleared dental device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242542
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. Medentika CAD/CAM Abutments (K242542) cites 5 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K223113 | Medentika Abutment System, Medentika CAD/CAM Abutments, Med... | Medentika GmbH | 2024 |
| K221301 | DESS Dental Smart Solutions | Terrats Medical SL | 2023 |
| K191123 | Multi-unit Abutments | Medentika GmbH | 2020 |
| K170838 | Medentika CAD/CAM TiBases | Medentika GmbH | 2017 |
| K150203 | Medentika CAD/CAM Abutments | Medentika GmbH | 2015 |
Trace the full predicate network for K242542
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.