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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