Orthorebirth Co., Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Orthorebirth Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: ReBOSSIS
4
Total
4
Cleared
0
Denied
Orthorebirth Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in San Diego, US.
Latest FDA clearance: Mar 2024. Active since 2014. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Orthorebirth Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mcra, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Orthorebirth Co., Ltd.
4 devices