Igi Laboratories, Inc. is one of 19743 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Igi Laboratories, Inc. - FDA 510(k) Cleared Devices
Recent clearances: HYALMIX CREAM, DERMISEB CREAM
2
Total
2
Cleared
0
Denied
Igi Laboratories, Inc. has 2 FDA 510(k) cleared medical devices. Based in Buena, US.
Historical record: 2 cleared submissions from 2013 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Igi Laboratories, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Beach Products, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Igi Laboratories, Inc.
2 devices