Form 8-K

8-K — Microbot Medical Inc.

Accession: 0001493152-26-048640

Filed: 2026-10-27

Period: 2026-10-27

CIK: 0000883975

SIC: 3841 (SURGICAL & MEDICAL INSTRUMENTS & APPARATUS)

Item: Regulation FD Disclosure

Item: Financial Statements and Exhibits

Documents

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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)

the Securities Exchange Act of 1934

Date

of Report (Date of earliest event reported): October 27, 2026

MICROBOT

MEDICAL INC.

(Exact

name of registrant as specified in its charter)

Delaware

000-19871

94-3078125

(State

or other jurisdiction

incorporation)

(Commission

File

Number)

(IRS

Employer

Identification

No.)

175

Derby St., Bld. 27

Hingham,

MA 02043

(Address

of Principal Executive Offices) (Zip Code)

Registrant’s

telephone number, including area code: (781) 875-3605

(Former

Name or Former Address, if Changed Since Last Report)

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

Common

Stock, $0.01 par value

MBOT

The

Nasdaq Stock Market LLC

Indicate

by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR §230.405)

or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2).

Emerging

Growth Company ☐

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.

October 27, 2026, Microbot Medical Inc. (the “Company”) disseminated a press release announcing that ELMNT IR, a multisite

outpatient interventional radiology practice in California, has signed an order to purchase up to a 12-month supply of the Company’s

LIBERTY Endovascular Robotic System devices. ELMNT IR became the first Office-Based Laboratory customer in the world to utilize the LIBERTY

Endovascular Robotic System, and the Company’s first customer on the West Coast. A copy of the press release is furnished as Exhibit

99.1 to this Current Report on Form 8-K.

The

information in this Item 7.01, including Exhibit 99.1, is being furnished and shall not be deemed to be “filed” for purposes

of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities

of that section, nor shall it be incorporated by reference into any filing under the Securities Act of 1933, as amended, or the Exchange

Act, regardless of any general incorporation language in such filing. By furnishing the information in this Current Report on Form 8-K

and Exhibit 99.1, the Company is making no admission as to the materiality of any information in this Item 7.01 or Exhibit 99.1.

Item

9.01. Financial Statements and Exhibits.

(d)

Exhibits

Exhibit

Number

Description

99.1

Press Release of Microbot Medical Inc., dated October 27, 2026

104

Cover

Page Interactive Data File (embedded within the Inline XBRL document)

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 thereunto duly authorized.

MICROBOT

MEDICAL INC.

By:

/s/

Harel Gadot

Name:

Harel

Gadot

Title:

Chief

Executive Officer, President and Chairman

Date:

October 27, 2026

EX-99.1

Filename: ex99-1.htm · Sequence: 2

Exhibit

99.1

Microbot

Medical® Secures its First Office-Based Lab (OBL) Customer for the LIBERTY® Endovascular Robotic System

ELMNT

IR also became the first account on the West Coast, marking a geographic expansion which aligns with the Company’s Full Market

Release strategy.

The

Company believes the OBLs represent a rapidly growing healthcare segment and opportunity as many endovascular procedures are being done

outside traditional hospital settings and Ambulatory Surgery Centers.

HINGHAM,

Mass., October 27, 2026 — Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY Endovascular

Robotic System, today announced that ELMNT IR, a multisite outpatient interventional radiology practice in California, has signed an

order to purchase up to a 12-month supply of LIBERTY devices. ELMNT IR became the first Office-Based Laboratory (OBL) customer in the

world to utilize the LIBERTY Endovascular Robotic System, and the Company’s first customer on the West Coast. An OBL is an outpatient

care setting that enables physicians to perform minimally invasive, image-guided procedures outside of the traditional hospital environment.

Jonathan

Steinberger, M.D., co-founder of ELMNT IR and a board-certified interventional radiologist specializing in minimally invasive, image-guided

treatments for vascular disease, cancer, men’s health conditions, and complex venous disorders, has already performed multiple

procedures using the LIBERTY System, including Y90 mapping, which is a planning procedure performed before Y-90 radioembolization, for

the treatment of liver tumors, Prostate Artery Embolization (PAE) for the treatment of benign prostatic hyperplasia (BPH), and Genicular

Artery Embolization (GAE) for symptomatic knee osteoarthritis.

“Having

used LIBERTY for multiple procedures, I’ve found that the combination of a compact footprint, efficient workflow, and the elimination

of upfront capital costs and expenses associated with traditional equipment makes LIBERTY an optimal system for establishing an Endovascular

Robotic Program in an OBL,” said Jonathan Steinberger, M.D., Co-Founder and Interventional Radiologist at ELMNT IR. “We have

seen firsthand the value it can bring to physicians and patients. Based on our experience to date, LIBERTY is well positioned to become

a standard for the use of robotics in endovascular intervention procedures.”

“This

is a significant milestone for us, and we believe it supports the value that LIBERTY brings across multiple sites of care settings, especially

in OBLs, as we believe they are an important and growing segment of the market,” commented Harel Gadot, Chairman, CEO, President.

“Our relationship with ELMNT IR, which has already resulted in advance orders of the LIBERTY System from ELMNT IR, continues a

trend in which every customer that has utilized its initial LIBERTY inventory has subsequently reordered additional systems. We believe

this reflects high satisfaction among physicians, as well as the acceptance by hospital administration, as they recognize the value of

the system. Furthermore, in addition to expanding access to healthcare networks, this represents an additional revenue opportunity for

the LIBERTY System as we expect the number of peripheral vascular interventions performed in OBLs to continue to increase.”

LIBERTY

is the only FDA cleared, single-use, remotely operated robotic system for peripheral endovascular procedures, and it is designed for

precise vascular navigation while aiming to reduce radiation exposure and physical strain.

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

relating 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, market acceptance of the LIBERTY system,

the length and outcome of hospital Value Analysis Committee and purchasing processes and the Company’s ability to convert sales

leads into orders, uncertainty in the results of regulatory pathways and regulatory approvals, uncertainty resulting from political,

social and geopolitical conditions, 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

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