STOCK TITAN

FOXO Technologies Inc. (OTC: FOXOD/FOXO) to acquire four U.S. blood centers

(High)
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

FOXO Technologies Inc., through its subsidiary Vector BioSource, Inc., has entered into a definitive agreement to acquire four U.S.-based blood collection centers from Grifols Bio Supplies, Inc. in an asset purchase including an upfront cash payment and a potential earnout tied to EBITDA targets in 2026, 2027 or 2028.

The acquisition is intended to create a proprietary source of bio-products and support new FDA licensure that is expected to expand Vector’s accessible market. Based on historical information and current estimates, FOXO states the acquisition should add over $10 million in net revenues during the twelve months following closing, although actual results may differ materially. Closing is anticipated in the third or fourth quarter of 2026, subject to customary closing conditions, including required FDA licensure and other regulatory authorizations.

Positive

  • None.

Negative

  • None.

Filing Explained

The acquisition agreement remains pending closing and includes an upfront cash payment whose amount is not stated in the provided disclosure; FOXO reported $65,896 of cash at March 31, 2026, equal to 10.3 days of first-quarter operating cash use.

Sources and calculations
  • Cash and equivalents vs quarterly operating cash outflow, in days of cash use $65,896 / ($577,898 / 90) = [object Object]
Item 7.01 Regulation FD Disclosure Disclosure
Material non-public information disclosed under Regulation Fair Disclosure, often investor presentations or guidance.
Item 9.01 Financial Statements and Exhibits Exhibits
Financial statements, pro forma financial information, and exhibit attachments filed with this report.
Blood collection centers acquired 4 centers Number of U.S.-based blood collection centers in the Vector BioSource acquisition agreement
Expected net revenues added over $10 million Projected net revenues during the twelve months following closing from the acquired centers
Earnout performance period 2026–2028 Earnout payable if EBITDA targets are reached in any of calendar years 2026, 2027 or 2028
Expected closing window Q3 or Q4 2026 Closing of the acquisition is anticipated in the third or fourth quarter of 2026, subject to conditions
Key regulatory approvals FDA licensure, CLIA certification, waste-management permit Approvals and permits cited as required for operating the acquired collection centers
definitive agreement regulatory
"Vector BioSource, Inc., has entered into a definitive agreement to acquire four"
A definitive agreement is a formal, legally binding document that outlines the final terms and conditions of a deal or transaction, such as a sale or partnership. It acts like a detailed contract that confirms all parties have agreed on the key details, making the deal official. For investors, it signals that the agreement is settled and moving toward completion, providing clarity and security about the transaction.
earnout payment financial
"consists of an upfront payment in cash and a potential future earnout payment"
An earnout payment is money a buyer agrees to pay a seller after a deal closes only if the acquired business hits certain future targets (such as revenue, profit, or milestones). It matters to investors because earnouts shift part of the purchase price onto future performance, affecting the buyer’s future cash flows and the seller’s incentives—like a performance bonus that reduces upfront risk but adds uncertainty about the true cost and value of the deal.
EBITDA financial
"earnout payment, payable if the acquired centers reach certain EBITDA targets"
EBITDA stands for earnings before interest, taxes, depreciation, and amortization. It measures a company's profitability by focusing on the money it makes from its core operations, ignoring expenses like taxes and accounting adjustments. Investors use EBITDA to compare how well different companies are performing financially, as it provides a clearer picture of operational success without the influence of financial structure or accounting choices.
CLIA certification regulatory
"failure to obtain the required new FDA licensure, CLIA certification, waste-management permit"
A CLIA certification is a U.S. federal approval that a laboratory must have to perform tests on human samples for diagnosis or monitoring. Think of it as a driver’s license for medical labs: it proves the lab meets standards for accuracy, reliability and quality control. Investors care because having or lacking CLIA certification affects a lab’s legal ability to generate test-related revenue, qualify for reimbursements, form partnerships, and avoid fines or shutdowns.
biospecimen technical
"evolving from a biospecimen sourcing company into a more integrated biospecimen solutions company"
A biospecimen is a biological sample taken from a person, animal, or the environment—such as blood, tissue, saliva, urine, or cells—used for testing, research, or diagnostic development. For investors, biospecimens are the essential raw material for creating drugs, diagnostics and lab tests; their availability, quality, legal consent and proper storage can speed or slow development and directly affect costs, regulatory approval chances and potential market value—like the foundation stones that determine how quickly a building can be completed.
Regulation FD regulatory
"the dissemination of such information is required by Regulation FD"
Regulation FD is a rule that prevents company insiders, like executives, from sharing important information with some people before others get it. It matters because it helps ensure all investors have equal access to key news, making the stock market fairer and reducing chances of insider trading.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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FAQ

What acquisition did FOXO (FOXO) announce involving Vector BioSource?

FOXO’s subsidiary Vector BioSource entered a definitive agreement to acquire four U.S.-based blood collection centers from Grifols Bio Supplies, Inc. The deal is structured as an asset purchase to secure proprietary bio-product supply for Vector’s customers.

How much revenue does FOXO (FOXO) expect from the Vector blood center acquisition?

FOXO expects the acquisition to add over $10 million in net revenues during the twelve months following closing. This projection is based on historical information and management estimates, and the company notes actual results may differ materially from these expectations.

What is the payment structure of FOXO’s (FOXO) Vector blood center acquisition?

The agreement includes an upfront cash payment plus a potential future earnout payment. The earnout is payable only if the acquired centers achieve specified EBITDA targets in any of calendar years 2026, 2027 or 2028, as defined in the agreement.

When is FOXO (FOXO) expecting the Vector blood center acquisition to close?

FOXO anticipates closing the acquisition in the third or fourth quarter of 2026. Completion is subject to customary closing conditions, including receipt of required FDA licensure and other regulatory authorizations for operating the blood collection centers.

What strategic benefits does FOXO (FOXO) see from acquiring blood collection centers?

The acquisition is intended to provide Vector with a proprietary source of bio-products and enable new FDA registrations and licensure. FOXO states these capabilities are expected to expand markets served and support integrated biospecimen solutions for biotechnology, diagnostics, pharmaceutical and research customers.

What key risks did FOXO (FOXO) highlight regarding the Vector acquisition?

FOXO cites risks including the ability to obtain financing for the cash purchase price, securing new FDA licensure, CLIA certification, waste-management permits, potential delays or failure to close, and the possibility that the centers may not achieve projected net revenues or EBITDA earnout thresholds.
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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934

 

Date of Report (Date Earliest Event Reported): July 29, 2026

 

FOXO TECHNOLOGIES INC.

(Exact name of registrant as specified in its charter)

 

Delaware   001-39783   85-1050265

(State or Other Jurisdiction

of Incorporation)

 

(Commission

File Number)

 

(IRS Employer

Identification No.)

 

477 South Rosemary Avenue
Suite 224
West Palm Beach , FL
  33401
(Address of Principal Executive Offices)   (Zip Code)

 

(612) 800-0059

(Registrant’s telephone number, including area code)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
N/A        

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.

 

 

 

 

 

 

Item 7.01. Regulation FD Disclosure.

 

On July 29, 2026, the Company issued a press release announcing that its subsidiary, Vector BioSource, Inc., has entered into a definitive agreement to acquire four U.S.-based blood collection centers from Grifols Bio Supplies, Inc., a U.S.-based subsidiary of Grifols S.A. A copy of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.

 

The information under this Item 7.01, including Exhibit 99.1 hereto, is being furnished herewith and shall not be deemed “filed” for the purposes of Section 18 of the Exchange Act, or otherwise subject to the liabilities of that section, nor shall such information be deemed incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange Act, except as expressly set forth by specific reference in such filing. Furthermore, the furnishing of information under Item 7.01 of this Current Report on Form 8-K is not intended to constitute a determination by the Company that the information contained herein, including the exhibit hereto, is material or that the dissemination of such information is required by Regulation FD.

 

Cautionary Statement Regarding Forward-Looking Statements

 

This Current Report on Form 8-K contains “forward-looking statements.” Any statements contained in this Current Report on Form 8-K that do not describe historical facts may constitute forward-looking statements. In some cases, you can identify forward-looking statements by terminology such as “if,” “may,” “should,” “expects,” “plans,” “anticipates,” “believes,” “estimates,” “predicts,” “potential” or “continue” or the negative of these terms or other comparable terminology. These forward-looking statements are based on information currently available to the Company’s management as well as estimates and assumptions made by its management and are subject to risks and uncertainties that may cause actual results, performance or developments to differ materially from those contained in the statements. These statements are only predictions and involve known and unknown risks, uncertainties and other factors, which may cause the Company’s or its industry’s actual results, levels of activity or performance to be materially different from any future results, levels of activity or performance expressed or implied by these forward-looking statements. These forward-looking statements are made as of the date of this Current Report on Form 8-K, and the Company does not undertake an obligation to update these forward-looking statements after such date.

 

Item 9.01 Financial Statements and Exhibits.

 

(d) Exhibits.

 

Exhibit

Number

  Description of Exhibit
99.1   Press Release Dated July 29, 2026
104   Cover Page Interactive Data File (formatted in Inline XBRL)

 

2

 

 

SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

  FOXO Technologies Inc.
     
Date: July 29, 2026 By: /s/ Seamus Lagan
  Name: Seamus Lagan
  Title: Chief Executive Officer

 

3

 

 

Exhibit 99.1

 

 

FOXO TECHNOLOGIES INC.’S SUBSIDIARY VECTOR BIOSOURCE, INC. ENTERS INTO DEFINITIVE AGREEMENT TO ACQUIRE FOUR BLOOD COLLECTION CENTERS FROM GRIFOLS BIO SUPPLIES, INC.

 

WEST PALM BEACH, FL, July 29, 2026 (GLOBE NEWSWIRE) — FOXO Technologies Inc.’s (OTC: FOXOD/FOXO) ( “FOXO”) subsidiary, Vector BioSource, Inc. (“Vector”) today announced that it has entered into a definitive agreement to acquire four U.S.-based blood collection centers (the “Agreement”) from Grifols Bio Supplies, Inc., a U.S.-based subsidiary of Grifols S.A. The acquisition is intended to provide a proprietary source of bio-products to sell to Vector’s customers to augment its existing sourcing model. Furthermore, the new FDA licensure that Vector expects to be required is anticipated to further expand Vector’s accessible market.

 

The Agreement, structured as a purchase of certain assets relating to four collection centers located in the United States, consists of an upfront payment in cash and a potential future earnout payment, payable if the acquired centers reach certain EBITDA targets (as defined in the Agreement) in any of calendar years 2026, 2027 or 2028. Based on historical information and management’s current estimates, the acquisition should add over $10 million in net revenues to FOXO during the twelve months following closing from the sale of whole blood, packed red blood cells, serum and other bio-samples, although actual results may differ materially. Further details on the acquisition can be found in the Company’s Form 8-K regarding the transaction, filed with the SEC on July 27, 2026.

 

The closing of the transaction is anticipated in the third or fourth quarter of 2026 and is subject to customary closing conditions including, but not limited to, the receipt of required FDA licensure and other regulatory authorizations.

 

Frank Dias, Jr., Chief Executive Officer of Vector stated, “This agreement marks an important milestone in the evolution of Vector. We are evolving from a biospecimen sourcing company into a more integrated biospecimen solutions company with our own blood collection capabilities that strengthen our supply chain and complement our established sourcing network. Beyond the acquisition itself, the opportunity to obtain the FDA registrations necessary to operate these collection centers and the FDA licensure required to support customers that require licensed collection facilities represents a significant strategic advancement for Vector. These regulatory capabilities are expected to expand the markets we can serve and enhance our ability to deliver comprehensive biospecimen solutions to the biotechnology, diagnostics, pharmaceutical and research communities. This transaction reflects our continued commitment to quality, compliance, operational excellence, and the creation of long-term value for our customers, partners, and shareholders.”

 

Seamus Lagan, Chief Executive Officer of Vector’s parent, FOXO, noted, “We are excited to support Vector’s rapid expansion and repositioning in the marketplace. In connection with the initial acquisition of Vector in September 2025, we felt strongly that Vector was an attractive platform in an exciting, high growth, high margin life science services sector.”

 

 

 

 

About FOXO Technologies Inc. (“FOXO”)

 

FOXO owns and operates four key subsidiaries.

 

Rennova Community Health, Inc., owns and operates Scott County Community Hospital, Inc. (d/b/a Big South Fork Medical Center), a critical access designated (CAH) hospital in East Tennessee.

 

Myrtle Recovery Centers, Inc., a 30-bed behavioral health facility in East Tennessee. Myrtle provides inpatient services for detox and residential treatment and outpatient services for MAT and OBOT Programs.

 

Vector BioSource, Inc. is an information, data and biospecimen sourcing provider serving the biotechnology, clinical research and pharmaceutical research industries.

 

FOXO Labs, Inc. is a biotechnology company dedicated to improving human health and life span through the development of cutting-edge technology and product solutions for various industries.

 

For more information about FOXO, visit www.foxotechnologies.com.

 

Forward-Looking Statements

 

This press release contains forward-looking statements that include words such as “expects,” “anticipates,” “believes,” “intends,” “plans,” “projects,” “estimates,” “may,” “will,” “should,” “could,” or similar expressions, are forward-looking statements. These statements are not historical facts, including statements about the FOXO’s beliefs and expectations, are forward-looking statements. Forward-looking statements involve inherent risks and uncertainties, and a number of factors could cause actual results to differ materially from those contained in any forward-looking statement. These factors include, but are not limited to the risk of changes in the competitive and highly regulated industries in which FOXO operates; variations in operating performance across competitors or changes in laws and regulations affecting FOXO’s business; the ability to implement FOXO’s business plans, forecasts, and other expectations; the ability to obtain financing to fund the cash purchase price of the acquisition; the risk that the acquisition may not close on the anticipated timeline, or at all, including as a result of the failure to obtain the required new FDA licensure, CLIA certification, waste-management permit or other regulatory authorizations; the risk that the acquired collection centers may not achieve the projected net revenues or the EBITDA levels necessary to trigger the earn-out payment; the risk that FOXO has a history of losses and may not achieve or maintain profitability in the future; the enforceability of FOXO’s intellectual property, including its patents and the potential infringement on the intellectual property rights of others; and the risk of downturns and a changing regulatory landscape in the highly competitive industries in which FOXO operates. The foregoing list of factors is not exhaustive. Readers should carefully consider the foregoing factors and the other risks and uncertainties discussed in FOXO’s most recent reports on Forms 10-K and 10-Q, particularly the “Risk Factors” sections of those reports, and in other documents FOXO has filed, or will file, with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and FOXO assumes no obligation and does not intend to update or revise these forward-looking statements, whether as a result of new information, future events, or otherwise.

 

No Offer or Solicitation

 

This press release is for informational purposes only and does not constitute an offer to sell, or a solicitation of an offer to buy, any securities of FOXO, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation, or sale would be unlawful. Any offer of securities will be made only by means of a registration statement or prospectus filed with, or an applicable exemption from the registration requirements of, the Securities Act of 1933, as amended.

 

Contact:

 

Sebastien Sainsbury

ssainsbury@foxotechnologies.com

(561) 485-0151

 

 

 

Filing Exhibits & Attachments

5 documents