510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935915Substantially Equivalent

Wet Sense

Edson Corp., Spring TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935915 is the FDA 510(k) clearance record for WET SENSE, a class II device, cleared for Edson Corp. on under FDA product code KPN (Alarm, Conditioned Response Enuresis). FDA records list one 510(k) clearance for Edson Corp. As of , FDA records show no recalls naming K935915.

Clearance record

Decision date
Received
(155 days to decision)
Product code
KPN Alarm, Conditioned Response Enuresis
Regulation
21 CFR 876.2040
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Edson Corp. 24015 Creek Wood Dr., Spring TX
510(k) summary
Summary
Third party review
No

Clearances, product code KPN

Trailing 12 months

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

FDA records show no clearances under product code KPN in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KPN, 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