The Lifestyle Company, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
The Lifestyle Company, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PuriLens Plus Preservative Free Saline
1
Total
1
Cleared
0
Denied
The Lifestyle Company, Inc. has 1 FDA 510(k) cleared medical devices. Based in Freehold, US.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by The Lifestyle Company, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Emergo Global Consulting, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - The Lifestyle Company, Inc.
1 devices