Lodox Systems (Pty), Ltd.

US Last updated 27 May 2026

Devices: 13
Registries: GUDIDFDA 510(k)FDA
FDA recalls: 0

Catalogue13

LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
Lodox eXero-dr Ref eXero-dr

Class II FDA UDI Active
LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
LODOX eXero-dr Ref eXero-dr

Class II FDA UDI Active
LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
LODOX eXero-dr Ref eXero-dr

Class II FDA UDI Active
Lodox eXero-dr Ref eXero-dr

Class II FDA UDI Active
LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
Lodox eXero-dr Ref eXero-dr

Class II FDA UDI Active
LODOX Xmplar-dr Ref Xmplar-dr

Class II FDA UDI Active
LODOX eXero-dr Ref eXero-dr

Class II FDA UDI Active
Lodox, Model Baseline Ref K013999

Class II FDA 510(k) Active

FDA establishments1

Registered with the FDA under this company group, matched by name.

Lodox Systems (Pty) Ltd. SANDTON Gauteng · ZA FEI 3003967489

What Lodox Systems (Pty), Ltd. makes

Lodox Systems (Pty), Ltd. manufactures stationary basic diagnostic x-ray systems that are digital in design. These systems are used for imaging purposes in medical settings and are identified by the device name LODOX or Lodox.

The company's devices are classified as Class II medical devices and are listed in the FDA's 510(k) database and the FDA's Unique Device Identification (UDI) system. Lodox Systems (Pty), Ltd. is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of devices does Lodox Systems manufacture?

Lodox Systems manufactures stationary basic diagnostic x-ray systems that are digital in design, such as the LODOX and Lodox systems, which are used for imaging purposes in medical settings.

Where is Lodox Systems based?

Lodox Systems is based in the United States.

Which registries list Lodox Systems' devices?

Lodox Systems' devices are listed in the FDA's 510(k) database and the FDA's Unique Device Identification (UDI) system.

How are Lodox Systems' devices classified?

Lodox Systems' devices are classified as Class II medical devices, indicating a moderate level of risk.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
DUNS number: 635684694

Catalogue13

LODOX Xmplar-dr Ref Xmplar-dr

Lodox eXero-dr Ref eXero-dr

LODOX Xmplar-dr Ref Xmplar-dr

LODOX eXero-dr Ref eXero-dr

LODOX Xmplar-dr Ref Xmplar-dr

LODOX Xmplar-dr Ref Xmplar-dr

LODOX eXero-dr Ref eXero-dr

Lodox eXero-dr Ref eXero-dr

LODOX Xmplar-dr Ref Xmplar-dr

Lodox eXero-dr Ref eXero-dr

LODOX Xmplar-dr Ref Xmplar-dr

LODOX eXero-dr Ref eXero-dr

Lodox, Model Baseline Ref K013999

FDA establishments1

What Lodox Systems (Pty), Ltd. makes

Frequently asked questions

Information