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
SUBSCRIBE / SIGN IN
K121833Substantially Equivalent

Ostomy Irrigation Set

MEDLINE INDUSTRIES, LP - Northfield, Plymouth MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K121833 is the FDA 510(k) clearance record for OSTOMY IRRIGATION SET, a class II device, cleared for Coloplast A/S on under FDA product code EXD (Irrigator, Ostomy). FDA records list 414 510(k) clearances for MEDLINE INDUSTRIES, LP - Northfield, from to . As of , FDA records show no recalls naming K121833.

Clearance record

Decision date
Received
(24 days to decision)
Product code
EXD Irrigator, Ostomy
Regulation
21 CFR 876.5895
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Coloplast A/S 1601 W. River Rd. N., Plymouth MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code EXD

Trailing 12 months

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

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