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Data / Medical devices / United States / The Lifestyle Co., Inc.

The Lifestyle Co., Inc.: FDA-registered device maker in Freehold, NJ, United States, 1 510(k) clearance

The Lifestyle Co., Inc. is registered with the FDA (registration 2249258) in Freehold, NJ, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated May 15, 2020. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number
2249258
FEI number
3002224304
Address
6 Paragon Way Ste 112, Freehold, NJ, United States, 07728
Owner or operator
The LifeStyle Company, Inc. (9035196)
Roles
Manufacturer
First device listed
October 2, 2020
Registered through
2026
Brand names listed
PuriLens Plus Preservative Free Saline

Devices it lists

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
May 15, 2020K200747PuriLens Plus Preservative Free SalineLPNSubstantially EquivalentThe Lifestyle Company, Inc.accessdata.fda.gov

Compare with other makers

Updated May 15, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.