Medical Device Manufacturer · US , Lenexa , KS

Labone, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2004

Total

Cleared

Denied

Labone, Inc. has 2 FDA 510(k) cleared medical devices. Based in Lenexa, US.

Historical record: 2 cleared submissions from 2004 to 2004. Primary specialty: Toxicology.

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

Labone, 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 - Labone, Inc.

2 devices

1-2 of 2