Lpi, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Lpi, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Solar Storm, Solar Wave, Sunco, and ESB (Avalon, Galaxy, Grande, Oasis, Elite and Leisure Select)
1
Total
1
Cleared
0
Denied
Lpi, Inc. has 1 FDA 510(k) cleared medical devices. Based in Johnson City, US.
Historical record: 1 cleared submissions from 2018 to 2018. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Lpi, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Lpi, Inc.
1 devices