Diode Laser Hair Removal WLA-01 (WINGDERM) – Labeling Issue (2024)
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Diode Laser Hair Removal model: WLA-01
Brand
WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China
Lot Codes / Batch Numbers
F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001
Products Sold
F7201110001 F1210910001 F1210910002 F7211210001 F7226110002 F7227110001
WINGDERM ELECTRO-OPTICS LTD. Room 312 Building D-3, Dongsheng Science Park, No.66 Of Xixiaokou Road, Haidian District Beijing China is recalling Diode Laser Hair Removal model: WLA-01 due to All model WLA-01 systems sold to US customers are found to have labeling non-compliances. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
All model WLA-01 systems sold to US customers are found to have labeling non-compliances
Recommended Action
Per FDA guidance
The firm sent a notification letter to the relevant distribution on June 6, 2024. Products sold before August 23, 2022, will require a software version upgrade to F1-B-1.1.012 or Higher.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026