510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K112268Substantially Equivalent

Codan Safefeed Enteral Feeding Reservoir

Codan US Corp., Santa Ana CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K112268 is the FDA 510(k) clearance record for CODAN SAFEFEED ENTERAL FEEDING RESERVOIR, a class II device, cleared for Codan US Corp. on under FDA product code KNT (Tubes, Gastrointestinal (And Accessories)). FDA records list 7 510(k) clearances for Codan US Corp., from to . As of , FDA records show no recalls naming K112268.

Clearance record

Decision date
Received
(224 days to decision)
Product code
KNT Tubes, Gastrointestinal (And Accessories)
Regulation
21 CFR 876.5980
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Codan US Corp. 3511 W. Sunflower Ave., Santa Ana CA
510(k) summary
Statement
Third party review
Yes

Clearances, product code KNT

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