510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K222969Substantially Equivalent

FERTI-LILY Conception Cup

Rosesta Medical BV, Amsterdam, NL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K222969 is the FDA 510(k) clearance record for FERTI-LILY Conception Cup, a class II device, cleared for Rosesta Medical BV on under FDA product code HDR (Cap, Cervical). FDA records list one 510(k) clearance for Rosesta Medical BV. As of , FDA records show no recalls naming K222969.

Clearance record

Decision date
Received
(269 days to decision)
Product code
HDR Cap, Cervical
Regulation
21 CFR 884.5250
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Rosesta Medical BV Mr. Treublaan 7 I, Amsterdam, NL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HDR

Trailing 12 months

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

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