Nibec Co., Ltd. is one of 19743 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nibec Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Regenomer® Syringe, Regenomer® Plug, Regenomer® Block, OCS-B COLLAGEN, GUIDOSS
3
Total
3
Cleared
0
Denied
Nibec Co., Ltd. has 3 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Historical record: 3 cleared submissions from 2014 to 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Nibec Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Smile US as regulatory consultant.
FDA 510(k) Regulatory Record - Nibec Co., Ltd.
3 devices