Prevent Products, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Prevent Products, Inc. makes
Prevent Products, Inc. manufactures passive and active venous return devices, including the Phlebopump Model 1000—a mechanical pump for reducing venous stasis—and ankle calf exercisers, both standalone and integrated with phlebopump functionality. These devices are designed to promote circulation and prevent deep vein thrombosis in patients at risk.
The company’s products are regulated under the FDA’s 510(k) pathway, with some classified as Class I and others as Class II. They are listed in the FDA’s 510(k) database, reflecting their authorised status under US medical device regulations. The company is based in the United States.
Catalogue
Phlebopump, Model 1000 Ref K003284
Regimes: 510(k) Registry: 510(k)Ankle Calf Exerciser Ref K942618
Regimes: 510(k) Registry: 510(k)Ankle Calf Exerciser Phlebopump Ref K952975
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Prevent Products, Inc. have in the registry?
The registry currently lists 3 devices for Prevent Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Prevent Products, Inc.'s devices?
Among its 3 most recently registered devices, Prevent Products, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Prevent Products, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Prevent Products, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Prevent Products, Inc. in the registry?
The most recently registered devices listed for Prevent Products, Inc. include PHLEBOPUMP, MODEL 1000, ANKLE CALF EXERCISER and ANKLE CALF EXERCISER PHLEBOPUMP.