510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K002154Substantially Equivalent

K.e.a.t.

Emd Electronic Medical Devices, Corp., Miami Beach FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K002154 is the FDA 510(k) clearance record for K.E.A.T., a class II device, cleared for Emd Electronic Medical Devices, Corp. on under FDA product code KPI (Stimulator, Electrical, Non-Implantable, For Incontinence). FDA records list one 510(k) clearance for Emd Electronic Medical Devices, Corp. As of , FDA records show no recalls naming K002154.

Clearance record

Decision date
Received
(248 days to decision)
Product code
KPI Stimulator, Electrical, Non-Implantable, For Incontinence
Regulation
21 CFR 876.5320
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Emd Electronic Medical Devices, Corp. 1621 Bay Rd., Suite 908, Miami Beach FL
510(k) summary
Summary
Third party review
No

Clearances, product code KPI

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