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Regenerative Medical Technology Group Inc reported $5.1M in revenue and a $7.8M net loss for fiscal 2025. See the full RMTG financial statements: income statement, balance sheet, cash flow and ratios, each column linked to its SEC filing.

Cellgenic Establishes Local Commercial Presence in Brazil

Cellgenic is deepening its on-the-ground commercial footprint in Brazil, pairing local support with ISSCA’s physician-education activity in São Paulo.

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Regenerative Medical Technology Group (RMTG) announced that its Cellgenic division has expanded its local commercial presence in Brazil through enhanced representation and physician-facing support. The buildout aims to strengthen physician relationships and support product distribution in permitted channels, while remaining fully subject to Brazilian law and ANVISA and other regulatory requirements.

Management treats Brazil as Cellgenic’s largest active Latin American expansion market and is shifting from a representation-only model toward a more permanent commercial footprint. The company links Cellgenic’s expanded Brazil operations with ISSCA’s ongoing physician-education conferences in São Paulo as a two-channel entry strategy focused on education and commercial infrastructure, with progress dependent on regulation, physician adoption, and available funding.

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Cellgenic is expanding local representation and commercial support in Brazil, one of Latin America's larger healthcare and aesthetic-medicine markets. ISSCA continues to hold physician-education events in São Paulo. Activities in Brazil remain subject to applicable local law and regulatory requirements.

MIAMI, FL / ACCESS Newswire / September 3, 2026 / Regenerative Medical Technology Group Inc. (the "Company" or "RMTG") (OTCID:RMTG), a regenerative medicine company operating through its wholly owned subsidiary Global Stem Cells Group, today announced that its Cellgenic division has expanded its commercial presence in Brazil through local representation, physician-facing commercial support, and related infrastructure intended to support product distribution in permitted channels. Brazil is an important healthcare and aesthetic-medicine market in Latin America.

The current Brazil buildout is intended to support physician relationships and longer-term market development. It does not, by itself, constitute regulatory approval of any product, a manufacturing facility in Brazil, or authorization to sell or administer any Cellgenic product other than as permitted under applicable Brazilian law, including requirements administered by ANVISA and other competent authorities. Brazil's scale and established community of physicians interested in regenerative medicine, together with ISSCA's periodic conference activity in São Paulo, are reasons management views Brazil as a priority market within Cellgenic's Latin American expansion plan.

Management currently treats Brazil as the largest of Cellgenic's active Latin American expansion markets and, for that reason, is moving from a representation-only model toward a more permanent local commercial presence. The timing, scope, and cost of that presence remain subject to execution, financing, and local regulatory requirements.

Operational and Strategic Update

David Christensen, Chief Executive Officer and President of Regenerative Medical Technology Group, Inc., commented: "Brazil is one of the largest and most sophisticated regenerative medicine markets in Latin America. A more permanent local commercial presence is intended to help Cellgenic develop longer-term physician relationships in that market."

Management believes the pairing of Cellgenic's expanded Brazil commercial operations with ISSCA's São Paulo conference activity illustrates RMTG's intended two-channel market entry - education and commercial infrastructure. Actual network development will depend on physician adoption, local regulation, and the Company's ability to fund and execute the plan.

About Regenerative Medical Technology Group, Inc.

Regenerative Medical Technology Group, Inc. (OTCID:RMTG) is a regenerative medicine company operating through Global Stem Cells Group and its subsidiaries, combining physician education, laboratory operations, biologics manufacturing, product commercialization, and digital healthcare technology across an international network. The Company operates across more than 30 countries. Additional information about the Company's business, operations, and risks is available in its filings with the Securities and Exchange Commission.

About Cellgenic

Cellgenic is the biologics and product-commercialization division of Global Stem Cells Group, developing and distributing advanced cellular technology, biologics, peptide therapeutics, and related regenerative-medicine products to physicians and clinics in permitted international markets, subject to applicable local regulatory requirements. Cellgenic products are not approved by the U.S. Food and Drug Administration, and the Company does not currently focus its commercial portfolio on the United States.

Forward-Looking Statements

This press release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Words such as "plan," "forecast," "anticipate," "estimate," "project," "intend," "expect," "should," "believe," "may," "will," "continue," and similar expressions are intended to identify forward-looking statements. These statements are based on management's current expectations and reflect management's current belief only.

Forward-looking statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties, and other factors that could cause actual results to differ materially from those expressed or implied, including, without limitation: the Company's ability to continue as a going concern; its liquidity position and need for additional capital; its substantial debt obligations and the risk of acceleration of that indebtedness; its history of operating losses; the Company's ability to form, staff, license, and fund local operations in Brazil; Brazilian regulatory, import, tax, currency, and reimbursement requirements, including ANVISA and professional-board rules applicable to biologics and cellular products; the risk that ISSCA educational events do not result in product sales or a durable physician network; regulatory developments in the United States, Argentina, Brazil, Mexico and the other jurisdictions in which the Company or its subsidiaries operate; market acceptance, operational execution, and competitive conditions; currency and general economic factors; potential dilution from existing and future equity or convertible instruments, including any increase in authorized capital; and the Company's ability to maintain compliance with applicable laws and the requirements of the OTC market. These and other risks are described more fully under "Risk Factors" in the Company's Annual Report on Form 10-K for the fiscal year ended December 31, 2025, and in its subsequent Quarterly Reports on Form 10-Q and other filings with the U.S. Securities and Exchange Commission, which are available at www.sec.gov. The Company undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events, or otherwise, except as required by law.

Information on or accessible through the Company's website, including RMTG.com, is not incorporated by reference into, and does not form a part of, this press release or the Company's filings with the Securities and Exchange Commission, which remain the authoritative source of information about the Company. This press release is for informational purposes only and does not constitute an offer to sell, or the solicitation of an offer to buy, any securities, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation, or sale would be unlawful.

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Contact:

Investor Relations
Regenerative Medical Technology Group, Inc.
ir@rmtg.com | (800) 956-3935
RMTG.com

SOURCE: Regenerative Medical Technology Group



View the original press release on ACCESS Newswire

FAQ

What did Regenerative Medical Technology Group (RMTG) announce about Cellgenic’s operations in Brazil?

RMTG announced that its Cellgenic division has expanded its commercial presence in Brazil through local representation, physician-facing commercial support, and related infrastructure designed to support product distribution in permitted channels, as part of its broader Latin American expansion focus.

Why is Brazil important for Cellgenic and RMTG (RMTG)?

The company treats Brazil as the largest of Cellgenic’s active Latin American expansion markets. Management cites Brazil’s scale, its established community of physicians interested in regenerative medicine, and ISSCA’s recurring São Paulo conferences as reasons Brazil is a priority market.

Does Cellgenic’s expanded presence in Brazil mean its products are approved there?

No. The company states that the Brazil buildout does not itself constitute regulatory approval of any product or authorization to sell or administer Cellgenic products beyond what is allowed under applicable Brazilian law, including requirements administered by ANVISA and other competent authorities.

What market-entry strategy is RMTG using for Cellgenic in Brazil?

Management describes a two-channel market-entry approach that pairs Cellgenic’s expanded commercial operations in Brazil with ISSCA’s physician-education conferences in São Paulo, combining education and commercial infrastructure to support longer-term physician relationships and market development.

Is Cellgenic moving to a permanent local commercial presence in Brazil for RMTG?

Yes. Management indicates it is moving from a representation-only model toward a more permanent local commercial presence in Brazil, though the timing, scope, and cost of that presence remain subject to execution, financing, and compliance with local regulatory requirements.

Are Cellgenic products approved by the U.S. FDA and is the U.S. a focus market for RMTG?

Cellgenic products are not approved by the U.S. Food and Drug Administration, and the company states that it does not currently focus its commercial portfolio on the United States, instead operating across more than 30 countries in permitted international markets.

What role does ISSCA play in RMTG’s Brazil strategy for Cellgenic (RMTG)?

ISSCA continues to hold physician-education events in São Paulo. Management believes combining ISSCA’s conference activity with Cellgenic’s expanded Brazil commercial operations supports its two-channel approach of education and commercial infrastructure to develop the regenerative-medicine market.