FDA 510(k)

MINT Product Family

K-Number: K192423 · 2020-09-09

Decision Date2020-09-09

Product CodeNEW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

MINT Product Family is a medical device manufactured by Hans Biomed Corporation. It received FDA 510(k) clearance on 2020-09-09 under approval number K192423. The device is classified under product code NEW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINT Product Family?

MINT Product Family is a medical device that received FDA 510(k) clearance on 2020-09-09. It is manufactured by Hans Biomed Corporation. The 510(k) number is K192423.

When was MINT Product Family approved by the FDA?

MINT Product Family received FDA 510(k) clearance on 2020-09-09, under approval number K192423.

What company makes MINT Product Family?

MINT Product Family is manufactured by Hans Biomed Corporation.

What is the FDA product code for MINT Product Family?

The FDA product code for MINT Product Family is NEW.

Other Devices by Hans Biomed Corporation

K171568SurFuse Gel, SurFuse Putty, ExFuse Gel, ExFuse Putty K220549MINT 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

Related Devices (Code: NEW)

K160705Y.JACOBS YOUNG'S THREAD Synthetic Absorbable Surgical Fixation Suture,Y. Jacobs Medical, Inc. K160761DW-1CDongwon Medical Co., Ltd. K150553FilblocAssut Europe K161737RELI REDIDIOX Dyed, RELI REDIDIOX, RELI REDIDIOX UndyedMyco Medical K172602MiracuFeeltech Co., Ltd. K181582DemeTECH DemeDIOX absorbable surgical sutureDemetech Corporation

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.