Ldi Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ldi Corporation - FDA 510(k) Cleared Devices
Recent clearances: FlexGard Cut-Resistant Glove Liners
1
Total
1
Cleared
0
Denied
Ldi Corporation has 1 FDA 510(k) cleared medical devices. Based in Portsmouth, US.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Ldi Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Quality & Regulatory Associates, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Ldi Corporation
1 devices