LiViliti Health Products Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
LiViliti Health Products Corporation - FDA 510(k) Cleared Devices
Recent clearances: Paptizer 360
1
Total
1
Cleared
0
Denied
LiViliti Health Products Corporation, develops General Hospital devices with a manufacturing facility in Lake City, US. The company specializes in smart sanitization technology for healthcare environments.
LiViliti has received 1 FDA 510(k) clearance from 1 total submission. The company's regulatory activity spans 2026, with its cleared device focused on General Hospital applications. Recent clearance demonstrates active engagement with FDA oversight.
The Paptizer 360 represents the company's core offering in hospital-grade sanitization. The device features UVC LED technology with extended operational lifespan and rapid sanitization cycles designed for clinical use.
Explore the company's FDA 510(k) clearance history, device names, and regulatory milestones in the database.
510(k) submissions have been managed by Nilo Medical Consulting Group as regulatory consultant.
FDA 510(k) Regulatory Record - LiViliti Health Products Corporation
1 devices