Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) (K242789)
Description
Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) by Dongguan Laiguang Electronic Technology Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K242789
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. Bestqool LED Therapy Device (LMK-001,LMK-004,LMK-005,LMK-006) (K242789) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K200983 | Infrared light therapy led facial light therapy mask-Derma ... | Ningbo Hesi Electric Co., Ltd. | 2021 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K251012 | TRUDERMAL Pro (ZLD-390) | Shenzhen Kaiyan Medical Equipment C... | 2025 |
Trace the full predicate network for K242789
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.