Class Class I
Luvis Chair (LC700C) (K233921)
Description
Luvis Chair (LC700C) by Dentis Co., Ltd., an FDA 510(k) cleared dental device.
Regulatory Information
Device ClassClass Class I
510(k) NumberK233921
Clearance Date2024-09-06
Clearance TypeTraditional
Product CodeKLC
Regulation Number872.6250
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K233921
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. Luvis Chair (LC700C) (K233921) cites 2 predicate devices and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K211556 | N2 | Megagen Implant Co., Ltd. | 2023 |
| K183347 | K3 | Osstem Implant Co., Ltd. | 2019 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K242611 | Integral Dental Units | Mipont Medical Equipment Co., Ltd. | 2025 |
Trace the full predicate network for K233921
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.