Orthoscan, Inc.
Orthoscan, Inc. holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2021, with 11 FDA device recalls on record.
Top product codes for Orthoscan, Inc.
FDA recalls by Orthoscan, Inc.
10 most recent of 11- Z-0574-2025 — Ziehm Solo FD. Interventional fluoroscopic x-ray system
- Z-0579-2025 — Ziehm Vision RFD 3D. Interventinoal fluoroscopic x-ray system
- Z-0577-2025 — Ziehm Vision R. Iterventional fluoroscopic x-ray system
- Z-0576-2025 — Ziehm Vision FD. Interventional fluoroscopic x-ray system
- Z-0578-2025 — Ziehm Vision RFD. Interventional fluoroscopic x-ray system
- Z-0575-2025 — Ziehm Vision system, x-ray, tomography, computed.
- Z-0573-2025 — Ziehm Solo. Digital Mobile C-arm
- Z-0259-2018 — Mobile Mini C-arm system Part # 1000-0004. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
- Z-0260-2018 — Mobile Mini C-arm system Part # 1000-0005. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
- Z-0258-2018 — Mobile Mini C-arm system Part # 1000-0001. Intended to provide the physician with general fluoroscopic visualization of the patient, including, but not limited to, surgical orthopedic procedures and critical and emergency care procedures.
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 Orthoscan, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.