Form 8-K

8-K — Microbot Medical Inc.

Accession: 0001493152-26-037031

Filed: 2026-08-11

Period: 2026-08-11

CIK: 0000883975

SIC: 3841 (SURGICAL & MEDICAL INSTRUMENTS & APPARATUS)

Item: Regulation FD Disclosure

Item: Financial Statements and Exhibits

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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): August 11, 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.

August 11, 2026, Microbot Medical Inc. (the “Company”) disseminated a press release announcing that it has filed its Quarterly

Report on Form 10-Q for the fiscal quarter ended June 30, 2026, and providing highlights of the Company’s second quarter ended

June 30, 2026. The press release is furnished herewith as Exhibit 99.1 and is incorporated herein by reference.

The

information in this Item 7.01, including the attached exhibit, 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 filings under the Securities Act of 1933, as amended, or the Exchange

Act, regardless of any incorporation by reference language of such filing. By furnishing the information in this Current Report on Form

8-K (“Form 8-K”) and the attached exhibit, the Company is making no admission as to the materiality of any information in

this Form 8-K or the exhibit.

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:

August 11, 2026

EX-99.1

Filename: ex99-1.htm · Sequence: 2

Exhibit

99.1

Microbot

Medical® Files 10-Q, Reports Significant Revenue and Customer Growth During the 2026 Second Quarter

Revenue

increased by more than 100% over prior fiscal quarter, driven by repeat orders, expanded utilization among existing customers, and the

acquisition of new customers since the Full Market Release in mid-April.

The

Company added new customers in Q3 while expanding into new states and sites of service.

HINGHAM,

Mass., August 11, 2026 — Microbot Medical Inc. (Nasdaq: MBOT), developer and distributor of the innovative LIBERTY® Endovascular

Robotic System, announced that it has filed its Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2026 with the Securities

and Exchange Commission (SEC). As disclosed in its July 7, 2026 press release, the Company generated greater than 100% revenue and customer

growth compared to the first quarter ended March 31, 2026.

Second

Quarter Highlights

●

Commenced the Full Market Release (FMR) of the LIBERTY System

during The Society of Interventional Radiology (SIR) Annual Scientific Meeting in April 2026.

●

New health systems in Massachusetts, North Carolina, Michigan,

and Pennsylvania adopted the LIBERTY System, joining Georgia, Florida, and New York, which adopted the LIBERTY System during the Limited

Market Release (LMR).

●

Increased the number of hospital sites using the LIBERTY System

across existing customer health systems.

●

Procedure volume increased in the second quarter ended June

30, 2026, compared to the first quarter ended March 31, 2026, as customers expanded deployment to additional sites and migrated more

users to the LIBERTY System.

●

The LIBERTY System was used across a variety of procedure types,

including Prostatic Artery Embolization (PAE), Y-90 Radioembolization, Genicular Artery Embolization (GAE) and Uterine Artery Embolization

(UAE), showcasing the versatility of the LIBERTY System.

●

Total revenue was

up more than 100% compared to the first quarter of 2026.

●

Having successfully completed the Limited Market Release in

April 2026, and with its associated costs partially being accounted for in the second quarter of 2026, coupled with other cost reduction

activities which are being implemented, the Company believes it will substantially reduce its cost of revenue which increased in the

three-month period ended June 30, 2026 compared to the three-month period ended March 31, 2026.

●

Entered into an agreement with Lovell Government Services Inc.

to serve federal healthcare systems, enabling access to more than 2,000 government healthcare facilities.

●

High customer satisfaction is reported and reflected in repeat

customer orders for the LIBERTY System as more sites and users are trained on the system.

●

Broadened its sales footprint to eight sales territories compared

to four sales territories at the end of March 2026, allowing the Company to be on track to have 12 territories across the U.S. by year-end.

●

Entered into an agreement with Sanmina and is in the process

of establishing a second manufacturing site to expand production capacity to support anticipated demand in the U.S. and international

markets, as well as future cost reduction initiatives.

●

Achieved a significant regulatory milestone as Israel became

the second jurisdiction — and the first outside of the U.S. — to grant marketing clearance for the LIBERTY System.

●

Awarded the 2026 Innovative Start-Up Award from Surgical Robotics

Technology (SRT), which recognizes companies with outstanding technological and commercial progress through highly innovative, groundbreaking

technologies.1

“We

achieved a number of key milestones during the second quarter and first half of 2026, including the successful transition from our Limited

Market Release to the Full Market Release earlier in the quarter,” commented Harel Gadot, CEO, President and Chairman. “This

resulted in the high growth we saw in both adoption and utilization, leading to a major increase in revenue from the prior period. We

are continuing to enhance our commercial team, expand our sales footprint, and to work closely with existing accounts to expand U.S.

sites and increase utilization. At the same time, we continue to implement cost reduction initiatives to lower the cost of revenues.

Internationally, we continue to establish a global infrastructure and implement our commercial readiness plans in Europe in anticipation

of obtaining a CE Mark.”

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

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, 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

https://www.surgicalroboticstechnology.com/surgical-robotics-industry-awards/categories/

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