Kick Ice, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kick Ice, Inc. makes
Kick Ice, Inc. manufactures disposable instant cold and hot packs designed for temporary thermal therapy. These products are intended for over-the-counter use to reduce swelling, relieve muscle soreness, or provide warmth for minor aches.
The company’s portfolio is regulated under FDA’s Class I device classification, with products listed via the 510(k) pathway. The products are distributed in the United States.
Catalogue
Instant Cold Pack Ref K963666
Regimes: 510(k) Registry: 510(k)Instant Hot Packs Ref K963768
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kick Ice, Inc. have in the registry?
The registry currently lists 2 devices for Kick Ice, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kick Ice, Inc.'s devices?
Among its 2 most recently registered devices, Kick Ice, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kick Ice, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kick Ice, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kick Ice, Inc. in the registry?
The most recently registered devices listed for Kick Ice, Inc. include INSTANT COLD PACK and INSTANT HOT PACKS.