Infralux International, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Infralux International, Inc. - FDA 510(k) Cleared Devices
2
Total
1
Cleared
0
Denied
Infralux International, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fairfield, US.
Historical record: 1 cleared submissions from 1987 to 1990. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Infralux International, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Infralux International, Inc.
2 devices