510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K122944Substantially Equivalent

Gemore True Sine Interferential Stimulator

Gemore Technology Co., Ltd., Tan Shui, New Taipei City, TW / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K122944 is the FDA 510(k) clearance record for GEMORE TRUE SINE INTERFERENTIAL STIMULATOR, a class II device, cleared for Gemore Technology Co, Ltd. on under FDA product code LIH (Interferential Current Therapy). FDA records list 14 510(k) clearances for Gemore Technology Co, Ltd., from to . As of , FDA records show no recalls naming K122944.

Clearance record

Decision date
Received
(88 days to decision)
Product code
LIH Interferential Current Therapy
Regulation
21 CFR 882.5890
Device class
Class II
Review panel
Neurology
Applicant
Gemore Technology Co, Ltd. 11 Floor , #29-5, Sec.2, Chung Cheng E. Rd.,, Tan Shui, New Taipei City, TW
510(k) summary
Summary PDF
Third party review
No

Clearances, product code LIH

Trailing 12 months

FDA records hold no clearances under product code LIH in the trailing twelve months.

FDA records show no clearances under product code LIH in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LIH, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260