510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K252831Substantially Equivalent

Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927)

Dolanvy (Suzhou) Medical Technology Co., Ltd, Suzhou, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K252831 is the FDA 510(k) clearance record for Pelvic Floor Treatment Device (DLR-8920, DLR-8921, DLR-8922, DLR-8923, DLR-8924, DLR-8925, DLR-8926, DLR-8927), a class II device, cleared for Dolanvy (Suzhou) Medical Technology Co., Ltd. on under FDA product code KPI (Stimulator, Electrical, Non-Implantable, For Incontinence). FDA records list one 510(k) clearance for Dolanvy (Suzhou) Medical Technology Co., Ltd. As of , FDA records show no recalls naming K252831.

Clearance record

Decision date
Received
(235 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
Dolanvy (Suzhou) Medical Technology Co., Ltd. Rm. 401, 402, Bldg. 1, # 69, Jiepu Rd., Suzhou, CN
510(k) summary
Statement
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