Orthorebirth Co., Ltd.
Orthorebirth Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Orthorebirth Co., Ltd.
FDA recalls by Orthorebirth Co., Ltd.
- Z-2132-2026 — ZENBONE, REF: ORB-0320C-Z, ORB-0310C-Z, ORB-0304C-Z
- Z-2131-2026 — BioCera Fibers, Bioresorbable Bone Void Filler, REF: ORB-0320C-KC, ORB-0310C-KC, ORB-0304C-KC, ORB-0302C-KC, ORB-0305D-KC
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Orthorebirth Co., Ltd.
Data sourced from openFDA. This site is unofficial and independent of the FDA.