Surgitech, Inc. is one of 25720 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Surgitech, Inc. - FDA 510(k) Cleared Devices
Recent clearances: CHRONIC PAIN SUPPRESSOR CPS-2000, MODEL CPS-2000, SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1
2
Total
2
Cleared
0
Denied
Surgitech, Inc. has 2 FDA 510(k) cleared medical devices. Based in Oceanside, US.
Historical record: 2 cleared submissions from 2003 to 2003. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by Surgitech, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Surgitech, Inc.
2 devices