STOCK TITAN

Microbot Medical® Increases Manufacturing Capacity as Demand for the LIBERTY® System Rises; Enters into Strategic Agreement with Sanmina, a Global Manufacturing Leader

(Very Positive)
Tags
partnership

Microbot Medical (Nasdaq: MBOT) signed a Letter of Agreement with Sanmina to manufacture the LIBERTY Endovascular Robotic System, the only FDA-cleared single-use, remotely operated robotic system for peripheral endovascular procedures.

The deal adds a second manufacturing site, aimed at boosting capacity, supporting global expansion, and, according to Microbot, improving operating efficiencies, lowering costs, and expanding gross margins as LIBERTY adoption grows in the U.S. and internationally.

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Positive

  • LOA with Sanmina adds a second manufacturing site for LIBERTY
  • Manufacturing expansion supports rising U.S. and international LIBERTY demand
  • Company targets lower costs and expanded gross margins via Sanmina partnership
  • Sanmina’s global footprint may support future LIBERTY production scale-up
  • Manufacturing move aligns with stated company cost reduction strategy

Negative

  • None.

News Market Reaction – MBOT

+4.28%
1 alert
+4.28% News Effect
+$5M Valuation Impact
$125.60M Market Cap
0.0x Rel. Volume

On the day this news was published, MBOT gained 4.28%, reflecting a moderate positive market reaction. This price movement added approximately $5M to the company's valuation, bringing the market cap to $125.60M at that time.

Data tracked by StockTitan Argus on the day of publication.

Market Context

This announcement underscores rising LIBERTY demand and a new Sanmina partnership to expand capacity...
Analysis

This announcement underscores rising LIBERTY demand and a new Sanmina partnership to expand capacity and support cost reduction. With prior updates often followed by weak trading and an active shelf in place, execution on scaling and margins remains a key watchpoint.

Key Figures

Revenue: $105,000 Net loss: $3.7 million Cash & equivalents: $3.7 million +5 more
8 metrics
Revenue $105,000 Q1 2026 LIBERTY sales
Net loss $3.7 million Quarter ended March 31, 2026
Cash & equivalents $3.7 million As of March 31, 2026
Marketable securities $68.8 million As of March 31, 2026
Shareholders’ equity $74.1 million As of March 31, 2026
Government facilities reach more than 2,000 facilities Potential LIBERTY access via Lovell agreement
Target procedures market approximately 2.5 million procedures annually U.S. peripheral endovascular procedures market
Shelf registration expenses $25,000.00 Listed issuance and distribution costs for S-3/A

Historical Context

5 past events · Latest: Jun 25 (Positive)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 25 Industry award Positive -1.1% LIBERTY System wins 2026 Innovative Start-Up Award, highlighting industry recognition.
Jun 23 Pennsylvania adoption Positive -1.6% First Pennsylvania health system adopts LIBERTY, expanding Eastern U.S. footprint.
Jun 16 Federal access deal Positive +0.0% Lovell Government Services agreement to open LIBERTY access across U.S. federal systems.
Jun 09 Michigan adoption Positive -2.5% First major Michigan health system adopts LIBERTY, first Midwest commercial account.
Jun 02 First NC customer Positive +1.5% First North Carolina academic health system adopts LIBERTY, broadening U.S. presence.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent positive commercial and adoption updates have often been followed by flat-to-negative next-day price moves.

Key Terms

endovascular, ce mark, gross margins, federal supply schedule, +2 more
6 terms
endovascular medical
"LIBERTY® Endovascular Robotic System, the only FDA-cleared single-use..."
Endovascular describes medical procedures performed inside blood vessels using thin tubes, wires, and implantable devices guided by imaging—like repairing a broken pipe from the inside rather than opening the wall. It matters to investors because these less-invasive techniques can shorten hospital stays, lower complication rates and create demand for specialized devices and imaging equipment, so changes in adoption, regulation or reimbursement can materially affect healthcare company revenues and margins.
ce mark regulatory
"progress towards obtaining CE Mark as well as registration in additional markets"
A CE mark is a regulatory stamp placed on products to show they meet the European Union’s basic safety, health and environmental rules and can be sold in the European Economic Area. For investors it matters because the mark unlocks market access, affects how quickly a product can generate revenue, and signals regulatory risk and potential compliance costs—think of it as a passport that lets a product enter a large market.
gross margins financial
"expects it will improve operating efficiencies, lower costs, and expand gross margins"
Gross margins measure the portion of sales a company keeps after paying the direct costs to make its products or deliver services, expressed as a percentage of revenue. Think of it as the money left from each sale after paying the ingredients — it signals how efficiently a business produces and prices goods, and matters to investors because higher margins generally mean more room to cover other expenses, invest, and generate profit.
federal supply schedule regulatory
"LIBERTY System is expected to be added to Lovell’s Federal Supply Schedule in Q3 2026"
A federal supply schedule is a government-approved list of products and services sold to federal agencies at pre-negotiated prices and terms, like a vetted catalog that agencies can order from without redoing contracts each time. For investors, being on such a schedule can mean steadier, predictable sales, lower marketing and sales costs to the government, and a competitive advantage that can help revenue grow more reliably over time.
form s-3 regulatory
"Amendment No. 1 to its Form S-3 registration statement"
Form S-3 is a legal document companies use to register their stock sales with the government, making it easier and faster for them to raise money by selling shares to investors. It’s like having a pre-approved shopping list that lets a company quickly sell new shares when they need funds, without going through a lengthy approval process each time.
rule 473(b) regulatory
"The amendment adds Rule 473(b) language for automatic effectiveness 20 days..."
Rule 473(b) is an SEC securities regulation that clarifies when written or graphic communications count as a prospectus for registered offerings, especially when they incorporate by reference material from a registration statement. For investors, that matters because it determines what information must be delivered or made available before a sale, and when liability for incomplete or misleading disclosures can attach—think of it as a rule that sets the ground‑truth for what written materials legally become part of the official offering documents.

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

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Expanding manufacturing capabilities is part of the Company’s cost reduction strategy and supports global expansion

HINGHAM, Mass., June 30, 2026 (GLOBE NEWSWIRE) -- Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY® Endovascular Robotic System, has entered into a Letter of Agreement (LOA) with Sanmina Corporation, a leading global integrated manufacturing solutions provider, to manufacture the LIBERTY System, the only FDA-cleared single-use, remotely operated robotic system for peripheral endovascular procedures. As momentum continues to rise in the U.S., reflected in increased accounts and usage across several states, and with the momentum building in the international markets as seen with the recent clearance in Israel and progress towards obtaining CE Mark as well as registration in additional markets, the Company believes it is necessary to expand its manufacturing capacity to meet expected demand from existing and new accounts as well as to support its cost reduction strategy.

“We are pleased and excited to mark the signing of this agreement,” said Asaf Shemesh, CEO, Sanmina Israel. “We are confident in the value of this partnership and what it represents for both organizations moving forward. We are eager and ready to support LIBERTY as it continues to grow and achieve its strategic objectives, while working together to ensure a successful and productive path forward.”

In addition to serving as a second site that diversifies the Company’s manufacturing capabilities, the Company expects it will improve operating efficiencies, lower costs, and expand gross margins. Furthermore, as one of the largest contract manufacturers globally, Sanmina has sites across many regions which could be beneficial as the Company scales production to meet anticipated demand over the next couple of years.

“As the pace of adoption continues to gain momentum, with several accounts across the Eastern U.S. increasing their utilization of the LIBERTY System and additional accounts in our existing and new sales territories are advancing in the sales funnel, we believe Sanmina will allow us to increase our manufacturing capacity and enable us to drive greater efficiency while addressing market demand for the foreseeable future,” commented Michal Ahuvia, Director of Operations. “With plans to increase our sales footprint to the Western U.S. later this year, along with recent clearance in Israel and current expectations for obtaining the CE Mark and other registrations, we believe securing a long-term partnership with a global leader like Sanmina positions us to meet expected near and long-term customer demand.”

About Microbot Medical

Microbot Medical Inc. (NASDAQ: MBOT) is a commercial stage medical device company focused on transforming endovascular procedures through advanced robotic technology. Microbot’s LIBERTY® Endovascular Robotic System is the first single-use, remotely operated robotic solution designed for precision, efficiency and safety. Backed by a strong intellectual property portfolio and a commitment to innovation, Microbot is driving the future of endovascular care.

Learn more at www.microbotmedical.com and connect on LinkedIn and X.

Safe Harbor

Statements to future financial and/or operating results, future adoption of products, future growth in research, technology, clinical development, commercialization and potential opportunities for Microbot Medical Inc. and its subsidiaries, along with other statements about the future expectations, beliefs, goals, plans, or prospects expressed by management, constitute forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 and the Federal securities laws. Any statements that are not historical fact (including, but not limited to statements that contain words such as “contemplates,” “continues,” “could,” “forecasts,” “intends,” “may,” “might,” “possible,” “potential,” “predicts,” “projects,” “should,” “would,” “will,” “believes,” “plans,” “anticipates,” “expects,” “estimates” and similar expressions) should also be considered to be forward-looking statements, but the absence of these words does not mean that a statement is not forward-looking. Forward-looking statements involve risks and uncertainties, including, without limitation, market conditions, risks inherent in the commercialization of the LIBERTY® Endovascular Robotic System, and in the development of future versions of or applications for the system, uncertainty in the results of regulatory pathways and regulatory approvals, uncertainty resulting from political, social and geopolitical conditions, particularly any changes in personnel or processes or procedures at the FDA and announcements of tariffs on imports into the U.S., disruptions resulting from new and ongoing hostilities between Israel and the Palestinians, Iran and other neighboring countries, and maintenance of intellectual property rights. Additional information on risks facing Microbot Medical® can be found under the heading “Risk Factors” in Microbot Medical’s periodic reports filed with the Securities and Exchange Commission (SEC), which are available on the SEC’s web site at www.sec.gov. Microbot Medical® disclaims any intent or obligation to update these forward-looking statements, except as required by law.

Contacts:
IR@microbotmedical.com
Media@microbotmedical.com


FAQ

What did Microbot Medical (MBOT) announce about its LIBERTY System manufacturing on June 30, 2026?

Microbot Medical announced a Letter of Agreement with Sanmina to manufacture its LIBERTY Endovascular Robotic System. According to Microbot Medical, this second site is intended to boost capacity, support global expansion, and enhance operating efficiency as demand grows.

How does the Sanmina agreement affect Microbot Medical (MBOT) manufacturing capacity?

The Sanmina agreement is intended to expand LIBERTY System manufacturing capacity through a second production site. According to Microbot Medical, this added capacity aims to meet expected demand from existing and new accounts in U.S. and international markets.

Why is Microbot Medical (MBOT) expanding LIBERTY System production with Sanmina?

Microbot Medical is expanding production to align with rising LIBERTY System usage and new market clearances. According to Microbot Medical, the strategy supports a cost reduction plan and is expected to improve operating efficiencies and gross margins while serving global demand.

What cost and margin benefits does Microbot Medical (MBOT) expect from the Sanmina partnership?

Microbot Medical expects the Sanmina partnership to improve operating efficiencies, lower costs, and expand gross margins. According to Microbot Medical, leveraging Sanmina as a major contract manufacturer supports its broader cost reduction strategy and anticipated LIBERTY demand over the next few years.

How does the Sanmina deal support Microbot Medical (MBOT) global expansion of the LIBERTY System?

The Sanmina deal provides manufacturing support that can scale across multiple regions. According to Microbot Medical, this complements recent Israel clearance and ongoing efforts toward CE Mark and other registrations, helping meet expected near- and long-term international LIBERTY System demand.

What role does LIBERTY System adoption in the U.S. play in Microbot Medical (MBOT) strategy?

Growing LIBERTY adoption in several Eastern U.S. accounts is a key driver of the manufacturing expansion. According to Microbot Medical, increased utilization and a planned sales footprint extension to the Western U.S. reinforce the need for higher production capacity.