Level-5, Inc. is one of 18344 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Level-5, Inc. - FDA 510(k) Cleared Devices
Recent clearances: NEPTUNE HYPERBARIC VENTILATOR
1
Total
1
Cleared
0
Denied
Level-5, Inc. is a medical device company with a manufacturing facility in Washington, DC. The company specializes in Anesthesiology devices for clinical use.
The company has received 1 FDA 510(k) clearance from 1 total submission. Level-5's regulatory history spans 2009, focusing on Anesthesiology devices. The company is currently inactive, with no clearances recorded in more than five years, and should be treated as a historical regulatory record.
Explore the company's cleared device names, product codes, and clearance dates in the database records above.
FDA 510(k) Regulatory Record - Level-5, Inc.
1 devices