Diode Laser Hair Removal Systems for Medical Use (Models: Milestone Smart-M, Milestone Standard-A)— 510(k) K222800

Substantially Equivalent

Sanhe Laserconn Tech Co., Ltd.

FDA 510(k) clearance K222800 for Diode Laser Hair Removal Systems for Medical Use (Models: Milestone Smart-M, Milestone Standard-A), Substantially Equivalent on 2022-11-07. Applicant: Sanhe Laserconn Tech Co., Ltd..

Clearance details

Applicant
Sanhe Laserconn Tech Co., Ltd.
Product code
Code GEX
Advisory panel
General, Plastic Surgery
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Langfang, CN
Download summary PDFView on FDA.gov ↗

Adverse events under product code GEX

product code GEX
Death
33
Injury
3,045
Malfunction
12,903
Other
25
Total
16,006

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.