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FDA 510(k) Applications Submitted by Hans Biomed Corporation
FDA 510(k) Number
Submission Date
Device Name
Applicant
K220549
02/25/2022
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
K171568
05/30/2017
SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty
Hans Biomed Corporation
K192423
09/04/2019
MINT Product Family
Hans Biomed Corporation
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