FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic
FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
$17,999
Genoray Zen‑7000 is a c-arm from Genoray. FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
Review technical facts, compatibility, included configuration and documentation before requesting a destination-specific B2B quotation.
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Genoray Zen‑7000 is a c-arm from Genoray, identified by model/part reference Zen‑7000. FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
Genoray Zen‑7000 is a c-arm from Genoray, identified by model/part reference Zen‑7000. FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
For procurement, confirm the exact Genoray Zen‑7000 label or serial identification, compatibility, included accessories and configuration against the written offer before installation or clinical/technical deployment.
Match Genoray Zen‑7000 model/part and serial or product-label details to the quotation.
Review host-system, accessory, software, power and facility requirements where relevant.
Confirm condition, included items, warranty, documentation and delivery terms before payment.
Use the final quotation and exact-unit photographs to confirm the supplied configuration and condition.

These model-specific points help buyers evaluate identity, compatibility and purchasing requirements.
FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
The FDA summary describes a C-arm plus workstation and lists a high-frequency generator, rotating X-ray tube, 9-inch image intensifier and 135° orbital rotation for the cleared configuration.
Verify exact generator/output configuration, image intensifier, workstation/software and DICOM features on the offered system.
Final suitability depends on the exact model configuration, compatible systems, professional use requirements and manufacturer instructions.
Evaluate Genoray Zen‑7000 for the professional use case supported by its documented equipment type and exact configuration.
Confirm required accessories, interfaces, software and facility requirements before deployment.
Useful for replacing a matching unit or expanding an existing equipment fleet after compatibility review.
Suitable for qualified institutional and B2B purchasing projects with exact-unit verification before shipment.
Use these details for product identification. Configuration-sensitive specifications should be checked against the exact supplied unit and manufacturer documentation.
Use this checklist to avoid configuration or compatibility mismatches.
Use authoritative documentation to confirm model identity, compatibility, operating requirements and configuration-sensitive details.
Technical or regulatory resource relevant to Genoray Zen‑7000 product evaluation.
Key questions for evaluating Genoray Zen‑7000 before purchase.
Genoray Zen‑7000 is a c-arm from Genoray. FDA 510(k) K103425 identifies the GENORAY ZEN-7000 as a mobile fluoroscopic X-ray imaging system.
Exact model, detector/image-intensifier configuration and serial number; Generator/tube and detector operating status; Workstation/software and DICOM options.
No. Hardware revision, software, accessories, probes, handpieces, modules or other options can vary. The written quotation and exact-unit identification should define the supplied configuration.
Only items explicitly listed in the quotation and packing scope should be treated as included. Reference photographs may show accessories or system components that are not part of the final offer.
International B2B delivery can be arranged for approved destinations subject to product-specific transport requirements, customs rules and the agreed Incoterms, freight and insurance conditions.
Manufacturer names and trademarks are used for product identification. Confirm model-specific instructions, compatibility and regional requirements before use.
Model, label/serial information, condition and supplied configuration can be confirmed before dispatch.
Quotation, packing scope, warranty terms and delivery responsibilities are documented before order approval.
Export packing, freight, insurance and shipment documentation can be coordinated for approved destinations.
Support is available for configuration questions, installation planning and procurement documentation.
Include delivery country, quantity, required configuration and target purchase date for a destination-specific offer.
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