Electro-Spec, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Electro-Spec, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Electro-Spec Steri-Caps
1
Total
1
Cleared
0
Denied
Electro-Spec, Inc. has 1 FDA 510(k) cleared medical devices. Based in Franklin, US.
Last cleared in 2023. Active since 2023. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Electro-Spec, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kapstone Medical as regulatory consultant.
FDA 510(k) Regulatory Record - Electro-Spec, Inc.
1 devices