The Lifestyle Company, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
What The Lifestyle Company, Inc. makes
The company manufactures PuriLens Plus, a preservative-free saline solution designed for contact lens care and disinfection.
This product is classified as Class II under FDA regulations and is listed via a 510(k) clearance. The company is based in the United States.
Catalogue
PuriLens Plus Preservative Free Saline Ref K200747
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Lifestyle Break Thru (Polymacon) Ref K965012
Regimes: 510(k) Registry: 510(k)Rigid Gas Permeable Contact Lenses Ref P900001
Regimes: PMA Registry: PMASgp Lens(Tm) Ref P840055
Regimes: PMA Registry: PMA
Frequently asked questions
How many devices does The Lifestyle Company, Inc. have in the registry?
The registry currently lists 5 devices for The Lifestyle Company, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list The Lifestyle Company, Inc.'s devices?
Among its 5 most recently registered devices, The Lifestyle Company, Inc. has devices listed in FDA 510(k) (3 devices) and FDA PMA (2 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do The Lifestyle Company, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for The Lifestyle Company, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from The Lifestyle Company, Inc. in the registry?
The most recently registered devices listed for The Lifestyle Company, Inc. include PuriLens Plus Preservative Free Saline, LIFESTYLE MV2 (TM) TORIC (POLYMACON) SOFT (HYDROPHILIC) MULTIFOCAL CONTACT LENS FOR DAILY WEAR (CLEAR OR TINTED), LIFESTYLE BREAK THRU (POLYMACON) and RIGID GAS PERMEABLE CONTACT LENSES.