Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Mobius Imaging

US

Last updated September 17, 2026

Information

Country
US
Address
2 Shaker Road, Shirley, MA, 01464
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
3010151377
DUNS Number
—

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Airo® MobiCT-32
FDA UDI
Class IIActive
Airo Ct System K131431
FDA 510(k)
Class IIActive
AIRO Computed Tomography (CT) X-ray System K180393
FDA 510(k)
Class IIActive
AIRO Computed Tomography (CT) X-ray System K160126
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (7)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Dec 4, 2025Z-1040-2026—open, classified

AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.

Dec 4, 2025Z-1041-2026—open, classified

AIRO pendant replacement kits and upgrade do not possess the "Safe Hand Position Warning" label.

Dec 7, 2022Z-0957-2023—open, classified

Stryker received one report of an injury to an untrained user that occurred while the untrained user was moving an Airo TruCT unit in reverse. The firm will increase visibility of instructions for users to consider when transporting the unit in reverse by providing labels to be affixed onto the AIRO.

Nov 18, 2022Z-0344-2023—terminated

Stryker received a report of a battery fire involving an Airo TruCT unit previously subjected to bypass charging. The firm is notifying customers with units whose battery monitoring systems were bypassed to charge the batteries; the batteries in these units require replacing.

Aug 1, 2018Z-2991-2018—terminated

The Tube Current Modulation feature (Modulated Scans) is not working in AIRO systems with software version 2.0.0.0, and operators would not be able to detect this fault until after a scan is completed.

Sep 26, 2017Z-0715-2018—terminated

If the tilt-drive motor has an intermittent connection or broken encoder or sensor wire there is a risk of unintended or unpredictable device motion while the CT system is homing the axis at startup or preparing for a scan.

Dec 8, 2014Z-1016-2015—terminated

There is a risk that during the transfer of an image and navigation data to the Brainlab Curve Image Guided Surgery Navigation System after a CT scan, an error may occur, causing either no navigation data or incorrect navigation data being transferred to the curve.