# K192423: MINT Product Family

- Pathway: 510(k) (Traditional)
- Applicant: Hans Biomed Corporation
- Decided: Sep 9, 2020 after 371 days
- Product code: NEW (Suture, Surgical, Absorbable, Polydioxanone)
- Device class: 2
- Regulation: 21 CFR 878.4840
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K142061 (2015). 2 ancestors in all.
4 later devices descend from it; 2 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K163676: Silhouette InstaLift, Silhouette Lift, Inc. (2017) Summary page 5.

## Most influential descendants
- K220549: MINT Product Family (Including MINT, MINT Lift, and MINT-I Sutures), MINT Lift ML 1043, MINT Lift ML 1013, MINT Lift 1019, MINT Lift Mini 1014 (2023), 2 descendants of its own
- K240389: Secret Line up (FCL18100C160  FCL19100E160 FCL1990E150  FCL2190G150 ); i-Thread (FCL18100C160  FCL19100E160 FCL1990E150  FCL2190G150) (2024), 1 descendant of its own
- K252171: Barbed PDO Suture (2026), 0 descendants of its own
- K242571: Secret Line up (FC1938E80 FC1950E90 FC1960E100 FC1970E120 FC1990E150 FC19100E150 FC19100E280 FC19100E420 FC2038E80 FC2050E90 FC2060E100 FC2070E120 FC2090E150 FC20100E170 FC2138G80 FC2150G90 FC2160G100 FC2170G120 FC2190G150 FC21100G170 FCL18100C160 FCL1938E80 FCL1950E90 FCL1960E100 FCL1970E120 FCL1990E150 FCL19100E160 FCL2138G80 FCL2150G90 FCL2160G100 FCL2170G120 FCL2190G150 FCL21100G160 FCRL1870C162 FCRL18100C185 FCRL1970E162 FCRL19100E185 FCHL1960E90 FCHL1970E120 FCHL19100E160 FCW1938 (2024), 0 descendants of its own

## Indications for use
MINT™ is indicated for use in mid-face suspension surgery to temporarily fixate the cheek subcutaneous fat layer and SMAS layer in an elevated position for the treatment of moderate to severe nasolabial folds.

Source page: https://510kreport.com/device/K192423
Methodology: https://510kreport.com/methodology