Medical Device Manufacturer · US , Morganville , NJ

The Lifestyle Co., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1997

Total

Cleared

Denied

The Lifestyle Co., Inc. has 2 FDA 510(k) cleared medical devices. Based in Morganville, US.

Historical record: 2 cleared submissions from 1997 to 2000. Primary specialty: Ophthalmic.

Browse the FDA 510(k) cleared devices submitted by The Lifestyle Co., Inc. Filter by specialty or product code using the sidebar.

The Lifestyle Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - The Lifestyle Co., Inc.

2 devices

1-2 of 2