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Turner Imaging Systems, Inc.

United States US-MF-000043549 Last updated 23 Oct 2026

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Devices
3
Registries
EUDAMEDGUDIDFDA
FDA recalls
0

Catalogue3

Authorised representatives

About

Turner's miniature x-ray devices are convenient and portable, designed to accommodate fast and flexible workflows.

From the manufacturer's own website. Source

What Turner Imaging Systems, Inc. makes

Turner Imaging Systems, Inc. manufactures portable miniature X-ray imaging devices, including the Smart-C system, its support stand, and a dedicated monitor cart for clinical use.

The company’s products are classified as Class I and Class IIb devices and are registered in the EU’s eudamed database. The manufacturer 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 types of medical devices does Turner Imaging Systems, Inc. manufacture?

Turner Imaging Systems, Inc. specializes in portable miniature X-ray imaging devices. Their product line includes the Smart-C X-ray system, a dedicated Smart-C Support Stand, and a Smart-C Monitor Cart, all designed for clinical use. These devices are intended to provide flexibility and convenience for imaging workflows.

Where is Turner Imaging Systems, Inc. based?

Turner Imaging Systems, Inc. is headquartered in the United States. The company’s U.S. location supports its focus on developing portable and compact X-ray imaging solutions tailored for clinical environments.

Which regulatory registries list Turner Imaging Systems, Inc.’s devices?

Turner Imaging Systems, Inc.’s devices are registered in the EU’s eudamed database. This registry is used to track medical devices authorized for placement on the European market, ensuring transparency and compliance with EU regulations.

How are Turner Imaging Systems, Inc.’s devices classified under medical device regulations?

Turner Imaging Systems, Inc.’s devices fall into two regulatory classifications: Class I and Class IIb. Class I devices generally pose minimal risk and may require fewer regulatory controls, while Class IIb devices involve a higher level of risk and require more stringent evaluation to ensure safety and performance.

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

Information

Country
United States
Address
1119 South 1680 West, Orem, United States
Phone
+1-801-796-2951
PRRC contact
Brad Allen
EUDAMED SRN
US-MF-000043549
FDA FEI number
3013099020