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Sign in to claim this brandFlow 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 36 of 67| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Wolf X-Ray | 65025LW-37 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66077TB-42 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68096TB-12 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62018LW-12 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66078TC-TB-14 | FDA UDI | Class I | Active |
| Flow Dental | 75090NL-18 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68101TB-22 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62018LW-41 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66081LW-23 | FDA UDI | Class I | Active |
| Coat Apron, Lead .5mm 25 X 40 | 63012-41 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62008TB-14 | FDA UDI | Class I | Active |
| Wolf X-Ray | 63011TB-19 | FDA UDI | Class I | Active |
| Coat Apron, Lead .5mm 24 X 40 | 63001-23 | FDA UDI | Class I | Active |
| Ink Align | RT-4426-OUVN | FDA UDI | Class I | Active |
| Wolf X-Ray | 67089LW-20 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62020LW-37 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66083TC-38 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68097LW-12 | FDA UDI | Class I | Active |
| Wolf X-Ray | 63013TB-12 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68093LW-14 | FDA UDI | Class I | Active |
| Wolf X-Ray | 65025TC-TB-20 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66078TC-TB-19 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68095LW-35 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66077TC-34 | FDA UDI | Class I | Active |
| Apronette, Standard Lead, 12" x 24" | 69097-39 | FDA UDI | Class I | Active |
| OR Quick Drop Apron Light Weight Lead | 68094LW-18 | FDA UDI | Class I | Active |
| Film Dss-57 D Adult Double Adult Butterfly Packets D Speed | 19601 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66078LW-22 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66080TC-TB-14 | FDA UDI | Class I | Active |
| Wolf X-Ray | 67090TB-19 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62018LW-14 | FDA UDI | Class I | Active |
| Apron and Vest, Men's Xtra Large, Standard Lead | 66084-25 | FDA UDI | Class I | Active |
| Minimax DUP-512 Duplicating Film | 20570 | FDA UDI | Class I | Active |
| Wolf X-Ray | 63011LW-12 | FDA UDI | Class I | Active |
| Easy Wrap Apron, Lead .5mm 24" X 42" | 65023-22 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66083TB-20 | FDA UDI | Class I | Active |
| Wolf X-Ray | 68091LW-34 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66080TC-TB-30 | FDA UDI | Class I | Active |
| Wolf X-Ray | 65027TB-38 | FDA UDI | Class I | Active |
| Wolf X-Ray | 66077TC-TB-20 | FDA UDI | Class I | Active |
| Special Procedure Apron, Standard Lead, Medium | 67087-39 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62018LW-42 | FDA UDI | Class I | Active |
| Wolf X-Ray | 62020TB-34 | FDA UDI | Class I | Active |
| Wolf X-Ray | 65027TC-TB-12 | FDA UDI | Class I | Active |
| Wolf X-Ray | 65026LW-37 | FDA UDI | Class I | Active |
| Easy Wrap Apron, Lead .5mm 25" X 40" | 65026-38 | FDA UDI | Class I | Active |
| Wolf X-Ray | 65027TC-TB-23 | FDA UDI | Class I | Active |
| Fv-58 Adult Econo Pak | 18215 | FDA UDI | Class I | Active |
| Patterson Dental | 20708 | FDA UDI | Class I | Active |
| Front Closing Spec. Procedure Apron, Standard Lead | 68095-20 | FDA UDI | Class I | Active |
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