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Virtual Imaging, Inc.

Also registered as Virtual Imaging

United StatesFDA applicant, unverified

Devices
9
FDA recalls
2

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Virtual Imaging, Inc. makes

Virtual Imaging, Inc. makes digital imaging systems for medical use, including fluoroscopy and radiography equipment such as the FLUOROPRO RF DIGITAL IMAGING SYSTEM and RADPRO ION. The company also produces devices like the CANON MODEL URS-50RF and CANON DIGITAL FLUOROSCOPY AND RADIOGRAPHY MODEL CXDI-50RF, which are digital fluoroscopy and radiography systems, as well as the CYPHER DICOM PRINT SOLUTION for medical image printing and management.

The devices manufactured by Virtual Imaging, Inc. are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

FDA recalls2

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 2 recalls initiated by Virtual Imaging, Inc., the earliest on 2014-09-22 and the most recent on 2018-11-02. By recorded status: 2 terminated. The reasons filed fall into these groups: mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

  • 2017 0
  • 2018 1
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0

1 initiated before 2017

  • 2018

    • 2 Nov 2018 Z-0460-2019 Class II Terminated There is a potential for the RadPRO Mobile 40kW Digital X-Ray System Model SM-40HF-B-D-C to separate from the Tube Head Mount and potentially fall off the system. Distribution: Worldwide Distribution - US Nationwide and the countries of, Canada, Italy Submission number: K101517

  • 2014

    • 22 Sep 2014 Z-1064-2015 Class II Terminated There is a potential for unintended and erratic motion. Distribution: USA (nationwide) to the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MO,…
      Full distribution text USA (nationwide) to the states of AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NH, NJ, NM, NY, OH, OK, OR, PA, SC, TN, TX, VA, WA, WI, WV) + US Army facility in South Korea; and the country of Canada.
      Submission number: K101517

Frequently asked questions

How many devices does Virtual Imaging, Inc. have in the registry?

The registry currently lists 9 devices for Virtual Imaging, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Virtual Imaging, Inc.'s devices?

Among its 9 most recently registered devices, Virtual Imaging, Inc. has devices listed in FDA 510(k) (9 devices).

What risk classes do Virtual Imaging, Inc.'s devices fall under?

Among its 9 most recently registered devices, the classes recorded for Virtual Imaging, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

Are there FDA recall records for Virtual Imaging, Inc.?

FDA recall records list 2 recalls initiated by Virtual Imaging, Inc., the most recent initiated on 2 Nov 2018. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Virtual Imaging, Inc. in the registry?

The most recently registered devices listed for Virtual Imaging, Inc. include AMX4-50 AND AMX4-31 MOBILE DIGITAL DIAGNOSTIC RADIOGRAPHIC SYSTEMS, VIEW(TM) IMAGE PROCESSING AND VIEWING STATION, VIEW 1000 and FLUOROPRO RF DIGITAL IMAGING SYSTEM.

Generated automatically from registry data and not verified by a human reviewer.