Class Class II
MegaGen Dental Implant Abutment (K242030)
Description
MegaGen Dental Implant Abutment by Megagen Implant Co., Ltd., an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK242030
Clearance Date2025-01-13
Clearance TypeTraditional
Product CodeNHA
Regulation Number872.3630
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242030
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. MegaGen Dental Implant Abutment (K242030) cites 7 predicate devices and is itself cited by 0 later devices.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K233450 | MegaGen Dental Implant Abutment - Scan Healing Abutment; Te... | Megagen Implant Co., Ltd. | 2024 |
| K231967 | ARi ExCon Implant System | Megagen Implant Co., Ltd. | 2023 |
| K203808 | Multi-unit Abutment, Multi-unit Angled Abutment | Megagen Implant Co., Ltd. | 2021 |
| K203554 | AnyOne External Implant System | Megagen Implant Co., Ltd. | 2021 |
| K182448 | AnyRidge Octa 1 Implant System | Megagen Implant Co., Ltd. | 2019 |
| K123988 | ANYONETM INTERNAL IMPLANT SYSTEM | Megagen Implant Co., Ltd. | 2013 |
| K110955 | ANYRIDGE INTERNAL IMPLANT SYSTEM | Megagen Co., Ltd. | 2011 |
Trace the full predicate network for K242030
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.