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PHT-70CHS is intended to produce panoramic, cephalometric, or 3D digital x-ray images. It provides diagnostic details of the dento-maxillofacial, sinus, and TMJ for adult and pediatric patients. The system also utilizes carpal images for orthodontic treatment. The device is to be operated by healthcare professionals.

The PHT-70CHS is a 4-in-1 digital X-ray system designed for both 2D and 3D dental radiographic imaging. The system integrates panoramic imaging, optional cephalometric imaging, dental computed tomography, and model imaging functions into a single unit. It is intended for dental diagnostic purposes and is capable of acquiring and processing multi-field-of-view digital radiographic images.

The PHT-70CHS is a complete digital radiographic imaging system that includes an X-ray generator, dedicated image receptors, and compatible image viewing software. The system supports acquisition of both 2D diagnostic images, including panoramic and cephalometric images, and 3D diagnostic images using cone beam computed tomography.

The materials, safety characteristics, X-ray source, indications for use, and image reconstruction including metal artifact reduction algorithms of the subject device are the same as those of the predicate devices PHT-75CHS (K231796) and PHT-90CHO (K243081).

Green X 12 VE and Green X VE are differentiated by the configuration of the CT and panoramic image receptors, which is reflected in their respective trade naming. Green X 12 VE is equipped with the Xmaru1404CF-PLUS Eth detector, while Green X VE is equipped with the Jupi0606X1 detector. Both configurations utilize the Xmaru2602CF Eth detector for cephalometric imaging.

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EzDent-i is dental imaging software that is intended to provide diagnostic tools for maxillofacial radiographic imaging. These tools are available to view and interpret a series of DICOM compliant dental radiology images and are meant to be used by trained medical professionals such as radiologist and dentist.

EzDent-i is intended for use as software to acquire, view, save 2D image files, and load DICOM project files from panorama, cephalometric, and intra-oral imaging equipment.

EzDent-i v3.5 is a device that provides various features to acquire, transfer, edit, display, store, and perform digital processing of medical images. EzDent-i is a patient & image management software specifically for digital dental radiography. It also provides server/client model so that the users upload and download clinical diagnostic images and patient information from any workstations in the network environment.

EzDent-i supports general image formats such as JPG and BMP for 2D image viewing as well as DICOM format. For 3D image management, it provides uploading and downloading support for dental CT Images in DICOM format. It interfaces with a 3D imaging software made by our company, the Ez3D-i (K131616, K150761, K161246, K163539, K173863, K190791, K200178, K211791, K222069, K231757) but the EzDent-i itself does not view, transfer or process 3D radiographs.

EzDent-i supports the acquisition of dental images by interfacing with OpenCV library to import the intra-oral camera images. It also supports the acquisition of CT/Panoramic/Cephalo/Intra-Oral Sensor /Intra-Oral Scanner images by interfacing with Xray capture software.

The provided text is a 510(k) summary for the EzDent-i/E2/Prora View/Smart M Viewer (v3.5) device. It asserts substantial equivalence to a predicate device (EzDent-i/E2/Prora View/Smart M Viewer v3.4). However, the document does not contain any specific acceptance criteria or details of a study proving the device meets acceptance criteria.

The "Performance Data" section (Section 10) only states: "SW verification/validation and the measurement accuracy test were conducted to establish the performance, functionality and reliability characteristics of the modified devices. The device passed all of the tests based on pre-determined Pass/Fail criteria. Also we have addressed the recommendations in the most recent cybersecurity guidance, "Cybersecurity in Medical Devices Quality System Considerations and Content of Premarket Submissions"."

This statement confirms that tests were conducted and passed, but does not provide the actual acceptance criteria, the reported device performance, sample sizes, details on ground truth establishment, expert qualifications, adjudication methods, or whether MRMC/standalone studies were performed.

Therefore, based solely on the provided text, I cannot complete the requested tables and information. The document confirms that testing occurred and passed, but the specifics required to answer your questions are not present in this 510(k) summary.

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