FDA 510(k)

Community Containers (Flap and Daisy)

K-Number: K252637 · 2025-10-14

Decision Date2025-10-14

Product CodeMMK

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

Community Containers (Flap and Daisy) is a medical device manufactured by Keter Canada, Inc.. It received FDA 510(k) clearance on 2025-10-14 under approval number K252637. The device is classified under product code MMK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Community Containers (Flap and Daisy)?

Community Containers (Flap and Daisy) is a medical device that received FDA 510(k) clearance on 2025-10-14. It is manufactured by Keter Canada, Inc.. The 510(k) number is K252637.

When was Community Containers (Flap and Daisy) approved by the FDA?

Community Containers (Flap and Daisy) received FDA 510(k) clearance on 2025-10-14, under approval number K252637.

What company makes Community Containers (Flap and Daisy)?

Community Containers (Flap and Daisy) is manufactured by Keter Canada, Inc..

What is the FDA product code for Community Containers (Flap and Daisy)?

The FDA product code for Community Containers (Flap and Daisy) is MMK.

Related Devices (Code: MMK)

K153274Med-Tainer Single Deposit ContainerSnyder Industries, Inc. K153363Red2Green Reusable Sharps ContainerTriumvirate Environmental, Inc. K161180Oak Ridge Products Sharps ContainersOak Ridge Products, LLC K152340NAR Sharps Shuttle; NAR Sharps Shuttle Pack of sixNorth American Rescue, LLC K170513MAUSER PG II Sharps ContainerMauzer USA, LLC K172719HealthBeacon HB2 Sharps BinHealthbeacon, Ltd.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.