Skip to content

Source-Ray, Inc.

United StatesFDA applicant, unverified FDA FEI 3004606964

Source-Ray, Inc. is a medical device manufacturer, with 21 devices listed in FDA GUDID and FDA 510(k) (FDA Class II and I) as of 13 Nov 2026.

Devices
21
Registrations
FDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • FDA GUDID 13
  • FDA 510(k) 8

A device listed in two registries counts in both.

Device classes
  • FDA Class II 16
  • FDA Class I 5
Identifiers
  • FDA FEI 3004606964
  • DUNS 113928654

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Source-Ray, Inc. makes

Source-Ray, Inc. manufactures mobile and stationary digital diagnostic x-ray systems, including generator units, x-ray tube housings, and remote control interfaces. Their portfolio includes standalone mobile units (e.g., SR-115-CG, SB-60-333) and portable x-ray systems (e.g., XRS-140-7.5K-P, PXS-710D) designed for basic radiography applications. Additional components like tube housings (e.g., SR-130-G, SR-1260-C) and universal control units (e.g., UC-5000) complement these systems.

The company’s devices are classified under FDA regulations as Class I or Class II, with submissions recorded in the FDA’s 510(k) and UDI registries. These products are intended for diagnostic imaging and are subject to U.S. medical device compliance requirements.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue21

Newest first, rows 1-21 of 21

Search and filter all 21 devices
Skip device list

  • Sr-115-Cg

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Sb-60-333

    Listed Registry: GUDID Class:I

  • Sr-130-G

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Xrs-140-7.5K-P

    Listed Registry: GUDID Class:I

  • Rc-115

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Sr-130-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Uc-5000

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Xrs-140-15K-P

    Listed Registry: GUDID Class:I

  • Sr-1260-C

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Sb-80-200R

    Listed Registry: GUDID Class:I

  • Sr-1260-G

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Pxs-710D

    Active Regimes: 510(k) Registry: GUDID Class:II

  • Xrs-125-7K-P

    Listed Registry: GUDID Class:I

  • Model Sr-115 Portable X-Ray System Ref K052001

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • UC-5000 Mobile X-Ray Ref K163063

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Podiatry X-Ray System Ref K133959

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Sr-130 Ref K030494

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Optional Remote Control, Model Rc-115, For Portable X-Ray System, Model Sr-115 Ref K062472

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Model Sr-130-D Portable Digital X-Ray System Ref K043062

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Pxs-810, Podiatry X-Ray System Ref K071392

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Portable X-Ray System, Model Powermax 1260 Ref K090655

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-21 of 21

Company details

FDA FEI number
3004606964
DUNS number
113928654
Address
50 Fleetwood Ct, Ronkonkoma, NY, 11779
Phone
631-244-8200

Frequently asked questions

How many devices does Source-Ray, Inc. have in the registry?

The registry currently lists 21 devices for Source-Ray, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Source-Ray, Inc.'s devices?

Among its 21 most recently registered devices, Source-Ray, Inc. has devices listed in FDA 510(k) (8 devices) and FDA GUDID (13 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Source-Ray, Inc.'s devices fall under?

Among its 21 most recently registered devices, the classes recorded for Source-Ray, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Source-Ray, Inc. in the registry?

The most recently registered devices listed for Source-Ray, Inc. include SR-115-CG, SB-60-333, SR-130-G and XRS-140-7.5K-P.

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