Class Class II
MOLLI 2 (K223107)
Description
MOLLI 2 by Molli Surgical, Inc., an FDA 510(k) cleared general, plastic surgery device.
Regulatory Information
Device ClassClass Class II
510(k) NumberK223107
Clearance Date2023-01-18
Clearance TypeTraditional
Product CodeNEU
Regulation Number878.4300
FDA Database
View on FDA DatabaseCategories
Predicate lineage for K223107
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. MOLLI 2 (K223107) cites 1 predicate device and is itself cited by 1 later device.
Predicate devices cited by this clearance
| K number | Device | Applicant | Year |
|---|---|---|---|
| K210600 | MOLLI | Molli Surgical, Inc. | 2021 |
Later devices that cite this one as their predicate
| K number | Device | Applicant | Year |
|---|---|---|---|
| K231579 | MOLLI 2 | Molli Surgical, Inc. | 2023 |
Trace the full predicate network for K223107
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.