Mobius Imaging, LLC
Mobius Imaging, LLC holds FDA 510(k) medical device clearances, first cleared 2013, most recent 2018, with 7 FDA device recalls on record.
Top product codes for Mobius Imaging, LLC
FDA recalls by Mobius Imaging, LLC
- Z-1041-2026 — Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.
- Z-1040-2026 — Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.
- Z-0957-2023 — MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography system.
- Z-0344-2023 — MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1
- Z-2991-2018 — AIRO Mobile CT System Model # MobiCT-32
- Z-0715-2018 — AIRO Mobile CT System, Model Number: MobiCT-32 Product Usage: The AIRO¿ is intended to be used for X-ray computed tomography applications for anatomy that can be imaged in the 107cm aperture excluding pediatric patients and patients weighing over 400 lbs. (182 kg).
- Z-1016-2015 — Airo Mobile Intraoperative CT I Airo; Model #: MobiCT-32. Computed Tomography x-ray system.
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 Mobius Imaging, LLC
Data sourced from openFDA. This site is unofficial and independent of the FDA.