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SUBJECT*
NX EQ Dental Radiographic Units, Intraoral (Internal X-Ray) (VA-26-00056583)
GENERAL INFORMATION
| CONTRACTING OFFICE’S ZIP CODE* |
| 21703 |
| SOLICITATION NUMBER* |
| 36C10X26Q0128 |
| RESPONSE DATE/TIME/ZONE |
| 04-23-2026 10:00am EASTERN TIME, NEW YORK, USA |
| ARCHIVE |
| 99 DAYS AFTER THE RESPONSE DATE |
SET-ASIDE
| PRODUCT SERVICE CODE* |
| 6515 |
| CONTRACTING OFFICE ADDRESS |
| Strategic Acquisition Center - Frederick |
Department of Veterans Affairs
5202 Presidents Court, Suite 103 Frederick MD 21703
POINT OF CONTACT*
Contract Specialist Jalima J. Jones Jalima.Jones@va.gov
PLACE OF PERFORMANCE
POSTAL CODE
COUNTRY
ADDITIONAL INFORMATION
| AGENCY’S URL |
| https://www.va.gov/opal/sac/index.asp |
| URL DESCRIPTION |
| VA | OALC | OPAL | SAC |
| AGENCY CONTACT’S EMAIL ADDRESS |
| Jalima.Jones@va.gov |
| EMAIL DESCRIPTION |
| Jalima.Jones@va.gov |
Sources Sought Notice Sources Sought Notice
DESCRIPTION
| *= Required Field |
| Sources Sought Notice |
Sources Sought Notice
1. DESCRIPTION
The Veterans Health Administration (VHA) Non-Expendable Equipment National Program has identified the Dental Radiographic Units Intraoral product line as a candidate for a VA-wide (otherwise referred to as “national”) single Requirements contract award.
The Department of Veterans Affairs’ (DVA) Office of Procurement, Acquisition and Logistics (OPAL) Strategic Acquisition Center (SAC) on behalf of VHA is issuing this Sources Sought Notice in accordance with the FAR 10.002(b)(2) to determine the availability and technical capabilities of qualified sources.
The SAC in conjunction with VHA is seeking a qualified source to provide Planmeca ProX™ brand name or equal to Dental Radiographic Units Intraoral on an agency wide basis. VA intends to award a Requirements Contract with Firm-Fixed Price (FFP) orders IAW FAR 16.503, Requirements Contract to a supplier of this equipment. Vendors will be required to deliver the Dental Radiographic Units Intraoral to VA medical centers and facilities throughout the United States and its territories.
The anticipated period of performance is for one 12-month base period with four 12-month option periods from the date of award. However, the Government's decision as to whether to continue with the contract, upon annual review, will be based upon successful performance during each previous year and continued need. The Contractor must demonstrate the ability to meet all requirements for the solicitation.
The associated North American Industrial Classification System (NAICS) code for this procurement is 339114 – Dental Equipment and Supplies Manufacturing, Product Service Code: 6515 – Medical and Surgical Instruments, Equipment, and Supplies. The FAR Provision found at 52.204-7(b)(1) requires that “All interested Offerors must be registered in SAM.gov prior to submitting an offer or quotation.” You may access the website at SAM.gov | Home. All offerors must be certified with the appropriate NAICS code on the SAM website. All SDVOSB/VOSB offerors must be verified in the SBA database at: https://veterans.certify.sba.gov/#search at the time of quote submission.
Submissions for this “source sought” shall be submitted by email no later than April 23rd, 2026, at 10:00 am EST to all the following:
Jalima.Jones@va.gov Kimberly.LeMieux@va.gov This notice is for planning purposes only and does not constitute a commitment on the part of the Government to award a contract, nor does the Government intend to pay for any information submitted as a result of this notice. This Sources Sought Notice is part of a continuous process for obtaining the latest information on the commercial status of the industry with respect to their current and near-term abilities. The information provided herein is subject to change and in no way binds the Government to solicit for, or award, a competitive contract. It is emphasized that this is a notice solely for planning and informational purposes.
2.0 SCOPE
Dental radiographic units are used for imaging dentition, individual tooth anatomy (i.e., crown, neck, root), and dental problems (e.g., caries) in adult and pediatric patients, as well as for orthodontic planning and assessment. Periapical radiographs capture the entire tooth and surrounding area, including the apex of the root; teeth in the maxillary arch and the mandibular arch are imaged separately. Periapical radiographs are used to examine the teeth, bone, and surrounding tissues. Pathological conditions such as a periapical abscess can be diagnosed and confirmed with this type of radiograph. Occlusal radiographs show the masticating surface of the premolars and molars.
The following Contract Line-Items Number (CLIN) are being considered:
| CLIN |
| Manufacturer |
| Part Number |
| Description |
| 0001 |
| Planmeca |
| PROXGO |
| ProX Go |
| 0002 |
| Planmeca |
| PROXSS-FC-60-NO or PROXSS-HC-60-NO |
| ProX Single Stud/Pass Thru 60" (w/Fixed CP or w/Handheld CP) |
| 0003 |
| Planmeca |
| PROXSS-FC-65-NO or PROXSS-HC-65-NO |
| ProX Single Stud/Pass Thru 65" (w/Fixed CP or w/Handheld CP) |
| 0004 |
| Planmeca |
| PROXSS-FC-70-NO or PROXSS-HC-70-NO |
| ProX Single Stud/Pass Thru 70" (w/Fixed CP or w/Handheld CP) |
| 0005 |
| Planmeca |
| PROXSS-FC-75-NO or PROXSS-HC-75-NO |
| ProX Single Stud/Pass Thru 75" (w/Fixed CP or w/Handheld CP) |
| 0006 |
| Planmeca |
| PROXSS-FC-80-NO or PROXSS-HC-80-NO |
| ProX Single Stud/Pass Thru 80" (w/Fixed CP or w/Handheld CP) |
| 0007 |
| Planmeca |
| PROXSS-FC-88-NO or PROXSS-HC-88-NO |
| ProX Single Stud/Pass Thru 88" (w/Fixed CP or w/Handheld CP) |
| 0008 |
| Planmeca |
| PROXDS-FC-60-NO or PROXDS-HC-60-NO |
| ProX Dual Stud 60" (w/Fixed CP or w/Handheld CP) |
| 0009 |
| Planmeca |
| PROXDS-FC-65-NO or PROXDS-HC-65-NO |
| ProX Dual Stud 65" (w/Fixed CP or w/Handheld CP) |
| 0010 |
| Planmeca |
| PROXDS-FC-70-NO or PROXDS-HC-70-NO |
| ProX Dual Stud 70" (w/Fixed CP or w/Handheld CP) |
| 0011 |
| Planmeca |
| PROXDS-FC-75-NO or PROXDS-HC-75-NO |
| ProX Dual Stud 75" (w/Fixed CP or w/Handheld CP) |
| 0012 |
| Planmeca |
| PROXDS-FC-80-NO or PROXDS-HC-80-NO |
| ProX Dual Stud 80" (w/Fixed CP or w/Handheld CP) |
| 0013 |
| Planmeca |
| PROXDS-FC-88-NO or PROXDS-HC-88-NO |
| ProX Dual Stud 88" (w/Fixed CP or w/Handheld CP) |
| 0014 |
| Planmeca |
| PROXSS-FC-60-ETH or PROXSS-HC-60-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 60" (w/Fixed CP or w/Handheld CP) |
| 0015 |
| Planmeca |
| PROXSS-FC-65-ETH or PROXSS-HC-65-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 65" (w/Fixed CP or w/Handheld CP) |
| 0016 |
| Planmeca |
| PROXSS-FC-70-ETH or PROXSS-HC-70-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 70" (w/Fixed CP or w/Handheld CP) |
| 0017 |
| Planmeca |
| PROXSS-FC-75-ETH or PROXSS-HC-75-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 75" (w/Fixed CP or w/Handheld CP) |
| 0018 |
| Planmeca |
| PROXSS-FC-80-ETH or PROXSS-HC-80-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 80" (w/Fixed CP or w/Handheld CP) |
| 0019 |
| Planmeca |
| PROXSS-FC-88-ETH or PROXSS-HC-88-ETH |
| ProX Single Stud/Pass Thru w/CTL Box 88" (w/Fixed CP or w/Handheld CP) |
| 0020 |
| Planmeca |
| PROXDS-FC-60-ETH or PROXDS-HC-60-ETH |
| ProX Dual Stud w/CTL Box 60" (w/Fixed CP or w/Handheld CP) |
| 0021 |
| Planmeca |
| PROXDS-FC-65-ETH or PROXDS-HC-65-ETH |
| ProX Dual Stud w/CTL Box 65" (w/Fixed CP or w/Handheld CP) |
| 0022 |
| Planmeca |
| PROXDS-FC-70-ETH or PROXDS-HC-70-ETH |
| ProX Dual Stud w/CTL Box 70" (w/Fixed CP or w/Handheld CP) |
| 0023 |
| Planmeca |
| PROXDS-FC-75-ETH or PROXDS-HC-75-ETH |
| ProX Dual Stud w/CTL Box 75" (w/Fixed CP or w/Handheld CP) |
| 0024 |
| Planmeca |
| PROXDS-FC-80-ETH or PROXDS-HC-80-ETH |
| ProX Dual Stud w/CTL Box 80" (w/Fixed CP or w/Handheld CP) |
| 0025 |
| Planmeca |
| PROXDS-FC-88-ETH or PROXDS-HC-88-ETH |
| ProX Dual Stud w/CTL Box 88" (w/Fixed CP or w/Handheld CP) |
| 0026 |
| Planmeca |
| PROSENSORUSB-S2-3FT or PROSENSORUSB-S2-6FT |
| ProSensor HD System Size 2 USB |
| 0027 |
| Planmeca |
| PROSENSORUSB-S1-3FT or PROSENSORUSB-S1-6FT |
| ProSensor HD System Size 1 USB |
| 0028 |
| Planmeca |
| PROSENSORUSB-S0-3FT or PROSENSORUSB-S0-6FT |
| ProSensor HD System Size 0 USB |
| 0029 |
| Planmeca |
| PROSENSORETH-S2-3FT or PROSENSORETH-S2-6FT |
| ProSensor HD System Size 2 Ethernet |
| 0030 |
| Planmeca |
| PROSENSORETH-S1-3FT or PROSENSORETH-S1-6FT |
| ProSensor HD System Size 1 Ethernet |
| 0031 |
| Planmeca |
| PROSENSORETH-S0-3FT or PROSENSORETH-S0-6FT |
| ProSensor HD System Size 0 Ethernet |
| 0032 |
| Planmeca |
| PROSENSORNC-S2-3FT or PROSENSORNC-S2-6FT |
| ProSensor HD Kit for ProX Size 2 |
| 0033 |
| Planmeca |
| PROSENSORNC-S1-3FT or PROSENSORNC-S1-6FT |
| ProSensor HD Kit for ProX Size 1 |
| 0034 |
| Planmeca |
| PROSENSORNC-S0-3FT or PROSENSORNC-S0-6FT |
| ProSensor HD Kit for ProX Size 0 |
| 0035 |
| Planmeca |
| 30056792 |
| ProSensor HD Sensor Only Size 2 -6' |
| 0036 |
| Planmeca |
| 30056791 |
| ProSensor HD Sensor Only Size 2 -3' |
| 0037 |
| Planmeca |
| 30056790 |
| ProSensor HD Sensor Only Size 1 -6' |
| 0038 |
| Planmeca |
| 30056787 |
| ProSensor HD Sensor Only Size 1 -3' |
| 0039 |
| Planmeca |
| 30056786 |
| ProSensor HD Sensor Only Size 0 -6' |
| 0040 |
| Planmeca |
| 30056785 |
| ProSensor HD Sensor Only Size 0 -3' |
| 0041 |
| Planmeca |
| 30056928 |
| ProSensor Control Box USB 6' |
| 0042 |
| Planmeca |
| 30056930 |
| ProSensor HD Control Box Ethernet |
| 0043 |
| Planmeca |
| 30056931 |
| ProX Sensor Control Box Retrofit |
The Department of Veterans Affairs (VA) is seeking vendors who can provide Planmeca ProX™ brand name, or equal to Dental Radiographic Units Intraoral as listed above or equal commodities which meet all the following salient characteristics (SCs):
SCs: Category 1 – Portable Handheld Intraoral X-Ray Unit
| SC # |
| SALIENT CHARACTERISTICS |
| Applicable CLIN |
| METHOD OF EVALUATION |
| SC 1 |
| Must be a portable handheld intraoral X-ray unit intended for dental intraoral radiographic imaging. |
| 0001 |
| Literature Review |
| SC 2 |
| Must provide image-quality performance suitable for intraoral dental radiography, including a focal spot size of 0.4 mm or smaller |
| 0001 |
| Literature Review |
| SC 3 |
| Must incorporate integrated radiation safety features for protection of both patient and operator. |
| 0001 |
| Literature Review |
| SC 4 |
| Must be battery powered and capable of cordless operation for portable clinical use. |
| 0001 |
| Literature Review |
| SC 5 |
| Must support portable chairside workflow in multiple treatment areas/operatories. |
| 0001 |
| Literature Review |
| SC 6 |
| Must be suitable for digital intraoral imaging workflows. |
| 0001 |
| Literature Review |
SCs: Category 2 – Fixed Intraoral X-Ray Unit
| SC # |
| SALIENT CHARACTERISTICS |
| Applicable CLIN |
| METHOD OF EVALUATION |
| SC 1 |
| Must be a fixed intraoral X-ray system intended for dental intraoral radiographic imaging. |
0002-0025 Literature Review
| SC 2 |
| Must support fixed installation in a dental operatory, such as wall, cabinet, pole, ceiling, or equivalent mounted configuration. |
0002-0025 Literature Review
| SC 3 |
| Must provide adjustable or selectable exposure settings suitable for intraoral imaging. |
| 0002-0025 |
| Literature Review |
| SC 4 |
| Must provide image-quality performance suitable for intraoral dental radiography, including a focal spot size of 0.7 mm or smaller. |
| 0002-0025 |
| Literature Review |
| SC 5 |
| Must support rectangular and circular collimation for intraoral dental imaging. |
| 0002-0025 |
| Literature Review |
| SC 6 |
| Tube head and arm assembly must allow positioning necessary for standard intraoral dental imaging. For wall mountings, arm extensions must be available to accommodate 85” length to dental treatment chair. |
0002-0025 Literature Review
| SC 7 |
| Must be suitable for digital intraoral imaging workflows, including compatibility with digital sensors and/or imaging plate systems. |
0002-0025 Literature Review
SCs: Category 3 – Digital Intraoral Sensor
| SC # |
| SALIENT CHARACTERISTICS |
| Applicable CLIN |
| METHOD OF EVALUATION |
| SC 1 |
| Must be a digital intraoral sensor suitable for routine dental intraoral radiographic imaging. |
| 0026-0043 |
| Literature Review |
| SC 2 |
| Must provide diagnostic quality imaging with high resolution and low-noise / high-contrast performance suitable for clinical diagnosis. |
| 0026-0043 |
| Literature Review |
| SC 3 |
| Must be offered in a configuration suitable for all patient intraoral imaging, whether through multiple sensor sizes or an ergonomic design intended to fit a wide range of patients. |
| 0026-0043 |
| Literature Review |
| SC 4 |
| Must support cleaning/disinfection and durable clinical use, including housing and cable design suitable for repeated use, including disinfection with intermediate-level hospital disinfectant with label claims of tuberculocidal activity. |
| 0026-0043 |
| Literature Review |
| SC 5 |
| Must connect through a standard computer interface such as USB, Ethernet, or equivalent manufacturer supported connection method. |
| 0026-0043 |
| Literature Review |
| SC 6 |
| Must be suitable for integration with commonly used dental imaging software or practice management/imaging environments. |
| 0026-0043 |
| Literature Review |
| SC 7 |
| Must furnish the standard accessories, drivers, and components necessary for clinical operation of the sensor. |
| 0026-0043 |
| Literature Review |
For each product (brand name and part number), the response must include descriptive literature demonstrating the product meets or exceeds the salient characteristics specified above.
The Government's intent is to include all ancillary items to ensure the equipment can function as designed by the Original Equipment Manufacturer (OEM) and as clinically required. Vendors are encouraged to provide any product solution or configuration so long as they meet the salient characteristics. Additionally, responses can include any additional product that may be beneficial. These items must be clearly identified by brand name and part number.
Responses to this Sources Sought Notice shall include the following:
1. Does vendor offer an annual service plan, Yes or No?
1. If Yes:
1. What does the plan cover?
1. Does plan cover software updates only?
1. Does the plan cover parts repair or replacement only?
1. Does the plan cover both software and parts?
1. Vendors are requested to provide documentation that shows information on their service plan.
1. Is the service provided by the OEM or a subcontractor?
1. Full name and address of company
1. CAGE Code/ SAM UIE
1. Business Size
1. Manufacturer or Distributor
7. If the distributor provides full name, business size and address of manufacturer.
1. Country of Origin designation for all products
1. Ability to provide uninterrupted supply of products on a national scale.
1. Technical Literature that clearly shows product(s) meets the identified salient characteristics and page numbers where each salient characteristic is met.
1. Any additional product solution or configuration that would be beneficial to the clinical functionality of the product line identified.
1. Authorized Distributor Letter Certified by OEM with a current date.
Although not required, vendors responding to this Sources Sought may also submit a Capabilities Statement.