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Shockwave Sources Sought

Closed HT940827Q0001 Special NoticeDefense Health Agency (DHA)
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At a glance

Defense Health Agency of Defense Health Agency (DHA) posted this Special Notice on Oct 8, 2026. Responses were due Oct 13, 2026; this notice is closed. NAICS 334510 (Electromedical and Electrotherapeutic Apparatus Manufacturing), product or service code Q520 (Professional - Toxicology). Place of performance: Texas 78236. Solicitation number HT940827Q0001.

Solicitation details

General information

Solicitation number
HT940827Q0001
Notice type
Special Notice
Place of performance
Texas 78236

Classification

NAICS
334510Electromedical and Electrotherapeutic Apparatus Manufacturing
Product or service
Q520Professional - Toxicology

Agency

Department
Department of Defense
Sub-tier
Defense Health Agency (DHA)
Office
Defense Health Agency

Description

From SAM.gov

The Healthcare Contracting Division - South is issuing this Sources Sought Notice on behalf of Wilford Hall Medical Center to find potential sources to obtain Shockwave Therapy equipment in that will provide both underwater electrical “spark gap” and an ellipsoidal reflector to concentrate shock-wave energy at a defined focal point in the target tissue. It must generate a high-energy acoustic shock wave   

THIS IS NOT A SOLICITATION ANNOUNCEMENT – This is a Sources Sought Notice and is issued solely for information and planning purposes – it does not constitute a Request for Quote (RFQ) or a promise to issue an RFQ in the future.  Solicitations are not available at this time and requests for a solicitation will not receive a response.  This notice does not constitute a commitment by the United States Government to contract for any supply or service whatsoever.  All information submitted in response to this announcement is voluntary; the United States Government will not pay for information requested nor will it compensate any respondent for any cost incurred in developing information provided to the United States Government.  Not responding to this Sources Sought Notice does not preclude participation in any future Request for Quote (RFQ), should one be issued.  It is the responsibility of the potential offerors to monitor this site for additional information pertaining to this requirement.

The Government will use responses to this notice in formulating its acquisition strategy. If the Government does not receive sufficient information in response to this notice to verify the potential for competition exists, it is possible that a sole-source contract, supported by a Justification and Approval document, will be issued to support the Government's requirement.  MRCO-W is seeking the following information (please answer paragraphs below with your response):

  1. Company name, UEI number, CAGE code, and point of contact information (including phone number and email address), and socio-economic category(ies) as related to NAICS 334510 (Electromedical and Electrotherapeutic Apparatus Manufacturing) or similar NAICS, such as 8(a), HUBZone, Women-Owned, Service-Disabled Veteran-Owned, Small, or Other-than-Small.

  1. Capability Statement (limited to ten pages), describing how your company meets the below objectives additional proof (such as product literature and locations where a system is currently installed) where appropriate:

The following are the minimum salient characteristics required by the Government:

a. The device must be a focused, electro-hydraulic shockwave therapy device capable of

reaching a high-energy Energy Flux Density (EFD) of at least >0.12 or >0.28 mJ/mm²

b. The device shall utilize an electro-hydraulic shockwave source.

c. The device shall provide a single treatment protocol.

d. The device shall be capable of performing up to ten (12) therapeutic sessions per day.

e. The device shall operate using a standard 120V electrical plug.

f. The extracorporeal shockwave therapy device shall be provided for clinical use in the treatment

of chronic musculoskeletal conditions, including but not limited to plantar fasciitis,

epicondylitis, calcific tendinopathy, and other clinically indicated soft-tissue disorders, as

determined by the Government’s licensed medical providers.

g. The device shall include documentation demonstrating greater than 80 percent effectiveness for  the intended treatment application(s), supported by published clinical data, manufacturer documentation, regulatory clearance documentation, or other evidence acceptable to the Government.

h. The device shall be in current serviceable condition and suitable for clinical use in a medical

treatment facility.

The response due date for this Sources Sought Notice is 4:00 PM CST, 13 October 2026.  All questions and comments regarding this announcement shall be submitted via e-mail to the below POCs:  YaKita McClurkin at yakita.s.mcclurkin.civ@health.mil.

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