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SYNTHES USA SALES, LLC

SYNTHES USA SALES, LLC is a federal contractor, registered under UEI HMFQYKJKLD93. It has been awarded $103,433,670 across 5,512 federal contracts. Primary work spans Surgical Appliance and Supplies Manufacturing, Surgical and Medical Instrument Manufacturing, and Medicinal and Botanical Manufacturing. Top awarding agencies include Department Of Veterans Affairs, Department Of Defense, and Department Of Defense (dod).

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HMFQYKJKLD93

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NAICS: 334510
New
Federal
Electro-Therapeutic Modalities for Pain Management (ETMPM) - Transcutaneous Electrical Nerve Stimulation (TENS) Procurement Program
Solicitation # 36C79126R0011
The Department of Veterans Affairs is soliciting proposals under Solicitation Number 36C79126R0011 to establish multiple single-award, Firm-Fixed-Price, Indefinite Delivery/Indefinite Quantity (IDIQ) contracts for the Electro-Therapeutic Modalities for Pain Management (ETMPM) program. This national procurement aims to provide FDA-cleared devices and accessories to support non-opioid pain management across 168 VA Medical Centers and over 1,000 Community-Based Outpatient Clinics. The scope includes Transcutaneous Electrical Nerve Stimulation (TENS) units, Interferential Current (IFC) units, Short-Wave Diathermy systems, and portable Neuromodulation devices for headache disorders, along with associated consumables such as electrodes and lead wires. The contract consists of a base year starting January 20, 2027, with four subsequent option years. The acquisition utilizes a Tiered Set-Aside Evaluation Approach, prioritizing Service-Disabled Veteran-Owned Small Businesses (SDVOSBs), followed by Veteran-Owned Small Businesses (VOSBs), other small businesses, and finally other-than-small businesses. Evaluation methodologies vary by item: CLINs X001 through X004 are awarded based on the Lowest Price Technically Acceptable (LPTA) method, while CLIN X005 is evaluated using a Best-Value Tradeoff approach, weighting technical factors at 60 percent, price at 25 percent, and past performance at 15 percent. All devices must be OEM-new and FDA 510(k) cleared for home use, with strict prohibitions against refurbished or gray-market products. Responsive proposals must be submitted via email by October 19, 2026, at 3:00 PM CDT and must include a signed SF 1449, a Technical Capability Statement, FDA clearance letters, and three past performance documents. Non-manufacturers are required to provide OEM-issued Authorized Distributor Letters. Additionally, offerors must submit a completed Price Matrix and mandatory certifications, including the Buy American Certificate and Trade Agreements Certificate. Product samples for every offered CLIN/SLIN must be shipped to the Denver Logistics Service facility in Golden, Colorado, by the proposal deadline.
Commodities & Services Acquisition Service (36C791)

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