Last synced on 25 January 2026 at 3:41 am

Diode Laser Hair Removal Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221312
510(k) Type
Traditional
Applicant
Guangzhou Chuang Zao Mei Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2022
Days to Decision
55 days
Submission Type
Summary

Diode Laser Hair Removal Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K221312
510(k) Type
Traditional
Applicant
Guangzhou Chuang Zao Mei Technology Co., Ltd.
Country
China
FDA Decision
Substantially Equivalent
Decision Date
6/29/2022
Days to Decision
55 days
Submission Type
Summary