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Flow X-Ray Corp.

US

Last updated May 23, 2026

What Flow X-Ray Corp. makes

Flow X-Ray Corp. manufactures radiation protection equipment for medical and dental imaging, including lead-lined aprons, reusable shielding pads, dental X-ray film (both screen and non-screen types), and X-ray intensifying screens. Their products are designed to reduce occupational and patient exposure during radiographic procedures.

The company’s portfolio consists of Class I medical devices, all listed in the FDA’s Unique Device Identifier (UDI) database. These products are intended for use in the US and comply with applicable regulatory requirements for radiation shielding and imaging materials.

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 Flow X-Ray Corp. manufacture?

Flow X-Ray Corp. specializes in radiation protection equipment for medical and dental imaging. Their product line includes lead-lined radiation shielding aprons, reusable patient shielding pads or drapes, dental X-ray film (both screen and non-screen types), and X-ray intensifying screens. These devices are designed to minimize radiation exposure for both healthcare professionals and patients during X-ray procedures.

Where is Flow X-Ray Corp. based, and what regulatory regions do their devices serve?

Flow X-Ray Corp. is based in the United States. Their devices are intended for use in the US market and are listed in the FDA’s Unique Device Identifier (UDI) database, which helps track and identify medical devices regulated by the FDA. The company’s products comply with applicable US regulatory requirements for radiation shielding and imaging materials.

Which regulatory registries or databases list Flow X-Ray Corp.’s devices?

Flow X-Ray Corp.’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. The UDI system is used to identify medical devices throughout their distribution and helps ensure traceability and regulatory compliance. This listing applies to all their products, which are classified as Class I devices.

How are Flow X-Ray Corp.’s devices classified under medical device regulations?

Flow X-Ray Corp.’s devices are classified as Class I medical devices. Class I devices are generally considered to pose the lowest risk and often involve minimal regulation beyond general controls. This classification applies to their radiation shielding equipment, including aprons, drapes, and X-ray film, as these products are designed to protect against radiation exposure without requiring invasive procedures or significant risk.

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

Information

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US
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Catalogue (3319)

Page 42 of 67
DeviceModel / ReferenceRegistriesClassStatus
Child Panoramic Apron .25mm 24" X 27" 75062NL-20
FDA UDI
Class IActive
Wolf X-Ray 66083TB-37
FDA UDI
Class IActive
Wolf X-Ray 10026
FDA UDI
Class IActive
Wolf X-Ray 67090LW-40
FDA UDI
Class IActive
Wolf X-Ray 68095TB-34
FDA UDI
Class IActive
Apronette, Standard Lead, 12" x 24" 69097-30
FDA UDI
Class IActive
Wolf X-Ray 68095TB-12
FDA UDI
Class IActive
Wolf X-Ray 66079TB-25
FDA UDI
Class IActive
Front Closing Special Procedure, Lead, Small 68091-12
FDA UDI
Class IActive
Child Panoramic Apron .3mm 24" X 27" 75062-39
FDA UDI
Class IActive
Thyroid Collar .3mm 5" X 27" 75056-23
FDA UDI
Class IActive
Flow Dental 75090-35
FDA UDI
Class IActive
Adult Panoramic Apron .25mm 24" X 27" 75061NL-36
FDA UDI
Class IActive
Child Bib Apron With Collar .3mm 20" X 20" 75053-12
FDA UDI
Class IActive
Wolf X-Ray 68100TB-12
FDA UDI
Class IActive
Front Closing Special Procedure, Lead, Small 68091-39
FDA UDI
Class IActive
Wolf X-Ray 68091TB-19
FDA UDI
Class IActive
Wolf X-Ray 66079TC-34
FDA UDI
Class IActive
Pro-Tek-To Pad 75057-35
FDA UDI
Class IActive
Wolf X-Ray 10028
FDA UDI
Class IActive
Special Procedure Apron, Standard Lead, Large 67088-34
FDA UDI
Class IActive
Wolf X-Ray 68100LW-39
FDA UDI
Class IActive
Wolf X-Ray 66077TB-25
FDA UDI
Class IActive
Wolf X-Ray 66083LW-41
FDA UDI
Class IActive
Wolf X-Ray 66079TC-TB-30
FDA UDI
Class IActive
Wolf X-Ray 62019LW-35
FDA UDI
Class IActive
Coat Apron, Lead .5mm 26 X 42 63013-22
FDA UDI
Class IActive
Special Procedure Apron, Standard Lead, Small 67086-22
FDA UDI
Class IActive
Wolf X-Ray 62018LW-30
FDA UDI
Class IActive
Coat Apron, Lead .5mm 26 X 42 63013-20
FDA UDI
Class IActive
Wolf X-Ray 68091LW-16
FDA UDI
Class IActive
Wolf X-Ray 68100TB-40
FDA UDI
Class IActive
Wolf X-Ray 66077TB-18
FDA UDI
Class IActive
Wolf X-Ray 63073TC-TB-16
FDA UDI
Class IActive
Apron, Bib .25mm 24x26 Teal 75050NL-14
FDA UDI
Class IActive
Wolf X-Ray 62018TB-40
FDA UDI
Class IActive
Front Closing Special Procedure, Lead, Small 68091-35
FDA UDI
Class IActive
Wolf X-Ray 63013TC-TB-34
FDA UDI
Class IActive
Apron and Vest, Men's Large, Standard Lead 66083-34
FDA UDI
Class IActive
Wolf X-Ray 67089LW-37
FDA UDI
Class IActive
Wolf X-Ray 66078TB-16
FDA UDI
Class IActive
Wolf X-Ray 68094TB-35
FDA UDI
Class IActive
Wolf X-Ray 66081TC-12
FDA UDI
Class IActive
Wolf X-Ray 66081TB-41
FDA UDI
Class IActive
Front Closing Spec. Procedure Apron, Standard Lead 68096-42
FDA UDI
Class IActive
Wolf X-Ray 63001LW-22
FDA UDI
Class IActive
Wolf X-Ray 62019TB-14
FDA UDI
Class IActive
Wolf X-Ray 68098TB-16
FDA UDI
Class IActive
Wolf X-Ray 65021TB-40
FDA UDI
Class IActive
Wolf X-Ray 63012TB-30
FDA UDI
Class IActive

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