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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record 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 · Hans Biomed Corporation · decided 2023-03-07 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
MINT LIFTMINT-I 40LC1940Hans Biomed Corp.NEW08809779587550
MINT LIFTMINT Lift MINI-S 1017Hans Biomed Corp.NEW08809779587574
MINT LIFTMINT-I 18WC1810Hans Biomed Corp.NEW08809779587536
MINT LIFTMINT Lift ML 1043Hans Biomed Corp.NEW08809779587581
MINT LIFTMINT-I 17WC1710AHans Biomed Corp.NEW08809779588946
MINT LIFTMINT-I 15WC1985Hans Biomed Corp.NEW08809779587543
MINT LIFTMINT 43BN1913Hans Biomed Corp.NEW08809779587567
MINTMINT-H 40LC1940Hans Biomed Corp.NEW08809963477858
MINTMINT-H 15WC1985Hans Biomed Corp.NEW08809963477445
MINTMINT-H 18WC1810Hans Biomed Corp.NEW08809963477384