Cherry Plastics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Cherry Plastics, Inc. makes
Cherry Plastics, Inc. manufactures medical device components, including the BITESTICK BLOCK—a connector block for medical gas systems—and the UNIVERSAL OXYGEN TUBING CONNECTOR, designed for secure and standardized oxygen delivery in healthcare settings.
These products are regulated under FDA 510(k) clearance and fall into Class I and Class II device classifications. The company is based in the United States.
Catalogue
Bitestick Block Ref K840789
Regimes: 510(k) Registry: 510(k)Universal Oxygen Tubing Connector Ref K840790
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cherry Plastics, Inc. have in the registry?
The registry currently lists 2 devices for Cherry Plastics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cherry Plastics, Inc.'s devices?
Among its 2 most recently registered devices, Cherry Plastics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Cherry Plastics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Cherry Plastics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cherry Plastics, Inc. in the registry?
The most recently registered devices listed for Cherry Plastics, Inc. include BITESTICK BLOCK and UNIVERSAL OXYGEN TUBING CONNECTOR.