510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K240247Substantially Equivalent

“MoFi” Cell Culture Basal Medium

Duogenic Stemcells Corporation, Taichung City, TW / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K240247 is the FDA 510(k) clearance record for “MoFi” Cell Culture Basal Medium, a class II device, cleared for Duogenic Stemcells Corporation on under FDA product code NDS (Media, Culture, Ex Vivo, Tissue And Cell). FDA records list one 510(k) clearance for Duogenic Stemcells Corporation. As of , FDA records show no recalls naming K240247.

Clearance record

Decision date
Received
(164 days to decision)
Product code
NDS Media, Culture, Ex Vivo, Tissue And Cell
Regulation
21 CFR 876.5885
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Duogenic Stemcells Corporation # 18, Ln. 10, Taiping 21st St., Taiping Dist., Taichung City, TW
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NDS

Trailing 12 months

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

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