510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K142794Substantially Equivalent

Everyway Facial MENS

Everyway Medical Instruments Co., Ltd., Shen Keng Hsiang, Taipei Hsien, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K142794 is the FDA 510(k) clearance record for Everyway Facial MENS, a class II device, cleared for Everyway Medical Instruments Co.,Ltd on under FDA product code NFO (Stimulator, Transcutaneous Electrical, Aesthetic Purposes). FDA records list 29 510(k) clearances for Everyway Medical Instruments Co.,Ltd, from to . As of , FDA records show no recalls naming K142794.

Clearance record

Decision date
Received
(246 days to decision)
Product code
NFO Stimulator, Transcutaneous Electrical, Aesthetic Purposes
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Everyway Medical Instruments Co.,Ltd 3fl, #5, Ln. 155, Sec. 3, Shen Keng Hsiang, Taipei Hsien, TW
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NFO

Trailing 12 months
9 clearances under product code NFO in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code NFO, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20260
April 20260
May 20262
June 20261
July 20261
August 20261
September 20262
October 20260