510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
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K232525Substantially Equivalent

Yoni.Fit Bladder Support

Watkins-Conti Products, Inc, Edmond OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K232525 is the FDA 510(k) clearance record for Yoni.Fit Bladder Support, a class II device, cleared for Watkins-Conti Products, Inc. on under FDA product code HHW (Pessary, Vaginal). FDA records list one 510(k) clearance for Watkins-Conti Products, Inc. As of , FDA records show no recalls naming K232525.

Clearance record

Decision date
Received
(270 days to decision)
Product code
HHW Pessary, Vaginal
Regulation
21 CFR 884.3575
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Watkins-Conti Products, Inc. 3841 E. Danforth Rd., Suite 109, Edmond OK
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HHW

Trailing 12 months
1 clearance under product code HHW in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code HHW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260