American Spine Center, Ltd. is one of 23669 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Spine Center, Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CLINI-LASE SYSTEM, MODELS CL-BASE, CL-2000, CL-1200, CL-500, CL-300, CL-275, CL-155, CL-55, CLP-BASE, CLP-275, CLP-55.
1
Total
1
Cleared
0
Denied
American Spine Center, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Belleville, US.
Historical record: 1 cleared submissions from 2005 to 2005. Primary specialty: Physical Medicine.
Browse the FDA 510(k) cleared devices submitted by American Spine Center, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Spine Center, Ltd.
1 devices