Form 8-K

8-K — Microbot Medical Inc.

Accession: 0001493152-26-018453

Filed: 2026-04-22

Period: 2026-04-22

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): April 22, 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

NASDAQ

Capital Market

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.

April 22, 2026, Microbot Medical Inc. (the “Company”) issued a press release highlighting that the Society of Interventional

Radiology (SIR) and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE), recently released updated joint guidelines

on occupational protection in interventional radiology. The revised guideline provides important safety guidance to physicians, radiographers,

nurses, medical physics experts, and all other staff involved in interventional radiology procedures, which could strengthen the commercial

position of the Company’s LIBERTY® Endovascular Robotic System.

The

press release, which is furnished as Exhibit 99.1 to this Current Report on Form 8-K, is incorporated herein by reference. The information

in this Item 7.01 and Exhibit 99.1 is being furnished and shall not be deemed to be “filed” for the purposes of Section 18

of the Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section. This report will not be

deemed an 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

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:

April 22, 2026

EX-99.1

Filename: ex99-1.htm · Sequence: 2

Exhibit

99.1

Microbot

Medical® Welcomes Updated Occupational Protection Guidelines from Leading Medical Societies, Strengthening Commercial

Position of LIBERTY®

Members

of the Society of Interventional Radiology (SIR) and the Cardiovascular and Interventional Radiological Society of Europe (CIRSE) Represent

the Largest Addressable User Market for the LIBERTY System

least Nine Medical Societies Endorse Updated Guidelines to Lower Radiation Exposure and Improve Ergonomic Issues Impacting Health Practitioners

HINGHAM,

Mass., April 22, 2026 — Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY®

Endovascular Robotic System, today highlighted that the Society of Interventional Radiology (SIR) and the Cardiovascular and Interventional

Radiological Society of Europe (CIRSE), recently released updated joint guidelines on occupational protection in interventional radiology.

The revised guideline provides important safety guidance to physicians, radiographers, nurses, medical physics experts, and all other

staff involved in interventional radiology procedures.

The

guidelines, which were published in CardioVascular and Interventional Radiology (CVIR), cover updated clinical evidence, new exposure

sources and address musculoskeletal risks for interventional radiology staff and, for the first time, include a section on radiation

protection during pregnancy for female practitioners.

“Part

of our mission for the LIBERTY System is to enable physicians to continue improving and saving patients’ lives while protecting

their own. LIBERTY’s design aims to reduce radiation exposure and physical strain for physicians and related medical staff, positioning

the LIBERTY System as a potential solution to address both the health, and the staffing challenges in interventional care,” commented

Harel Gadot, Chairman, CEO & President. “It is very encouraging to see increased emphasis on protecting healthcare providers

in the interventional space coming from leading medical societies, such as the American Medical Association (AMA), one of the largest

medical associations in the U.S., along with SIR and CIRSE.”

Prolonged

exposure to radiation may have significant long-term health risks, including cancer, cardiovascular disease, reproductive health effects,

and cataracts. These risks have also been cited as contributing to the staffing shortage in the endovascular space, especially in interventional

radiology, which currently ranks number two among specialties with highest physician shortages. The burden disproportionately affects

women, who often cite radiation exposure and the physical demands of wearing lead aprons as barriers to entering or advancing in the

field. The LIBERTY System’s remote operation capabilities enable physicians to work away from the radiation source and in a seated

position, potentially lowering musculoskeletal strain while improving workflow efficiency.

Along

with SIR and CIRSE, occupational protection initiatives are being endorsed by the Society of NeuroInterventional Surgery (SNIS), the

Society of Vascular and Interventional Neurology (SVIN), the Society for Cardiovascular Angiography and Interventions (SCAI), American

College of Cardiology (ACC), the Alliance for Cardiovascular Professionals (ACVP), the American Society of Echocardiography (ASE), the

Heart Rhythm Society (HRS), and Society for Vascular Surgery (SVS). Additionally, in late 2025,

the American Medical Association (AMA) adopted a new policy to strengthen protections for healthcare professionals and trainees who may

face occupational radiation exposure. The policy emphasizes the importance of continued research into the health effects of cumulative

exposure to ionizing radiation, as well as education and training to minimize occupational risk to physicians and patients.

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 world’s first FDA cleared 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

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