Stock Markets May 14, 2026 09:48 AM

Microbot Medical Shares Slide After Short Seller Flags Questions About LIBERTY Robot

Bearish research from White Diamond accuses device of being impractical, costly to use and lacking reimbursement support

By Maya Rios MBOT

Microbot Medical Inc. (NASDAQ:MBOT) shares fell sharply after a short-seller report from White Diamond Research raised doubts about the commercial prospects of the company's LIBERTY Endovascular Robotic System. The report, which includes interviews with surgeons and a disclosed short position, set a $1 price target and highlighted concerns over per-procedure costs, single-use hardware, guidewire compatibility and the absence of a specific reimbursement pathway.

Microbot Medical Shares Slide After Short Seller Flags Questions About LIBERTY Robot
MBOT

Key Points

  • Microbot Medical stock fell 7.8% after White Diamond Research published a negative report and disclosed a short position, assigning a $1 target.
  • Surgeons interviewed by the research firm reported added per-procedure costs of $3,000 to $4,000, longer case times and no accuracy advantage over manual procedures.
  • The device's single-use hardware, limited guidewire compatibility and lack of a specific reimbursement code raise commercial adoption concerns; this affects medical device and healthcare provider economics.

Shares of Microbot Medical Inc (NASDAQ:MBOT) declined 7.8% on Thursday after White Diamond Research published a bearish analysis questioning whether the company's LIBERTY Endovascular Robotic System can achieve commercial traction.

The research firm attached a $1 target to the stock and disclosed that it holds a short position. White Diamond said it spoke with surgeons who have experience with the LIBERTY system and found substantial reservations about the device's practicality in routine clinical use and its economic impact on hospital procedures.


Surgeon feedback and economics

In interviews cited in the report, an anonymous surgeon estimated the LIBERTY adds between $3,000 and $4,000 to the cost of a single procedure, and said that there is currently no reimbursement mechanism to cover that incremental expense. That surgeon also told the researchers that procedures take longer when using the robot and that it does not provide an accuracy advantage compared with manual techniques. The surgeon was quoted saying:

"it’s gonna be extra work for you. The case is gonna take longer. You could do this yourself without the robot faster, with equal accuracy. And it’s gonna cost you an extra $3,000."

The report also cites Dr. Charles Briggs of Tampa General Hospital, who told the researchers he employs the LIBERTY roughly once every week to week and a half. He indicated he is the only surgeon out of the hospital’s roughly 15 vascular surgeons who uses the device on a regular basis.


Device limitations and reimbursement challenges

White Diamond noted several technical and economic limitations. The LIBERTY system is only compatible with .014" guidewires, whereas most peripheral vascular procedures rely on .018" guidewires. Additionally, the research firm said the entire system - including the remote control and robotic drive unit - is disposed of after a single use, a factor that may add to per-case cost.

The report further highlights that the device lacks a dedicated reimbursement code. It also states the LIBERTY does not qualify for New Technology Add-on Payment status because, according to the authors, it has not demonstrated substantial clinical benefit for patients relative to standard procedures.


Company background referenced

White Diamond drew a comparison between Microbot Medical and XACT Robotics, another company founded by Microbot CEO Harel Gadot. The report states that XACT Robotics ceased operations in 2023 after failing to generate significant revenue despite having received FDA clearance.

Investors reacted to the report with a notable sell-off in the stock. The questions raised in the research note center on adoption hurdles, procedure economics and the absence of reimbursement support - all factors the report argues could limit commercial uptake.

Risks

  • Adoption risk: Low usage among vascular surgeons, as illustrated by one hospital where only one of approximately 15 vascular surgeons regularly uses the LIBERTY - this could hinder sales and revenue growth in the medical device sector.
  • Reimbursement uncertainty: The LIBERTY lacks a dedicated reimbursement code and does not qualify for New Technology Add-on Payment status per the report, creating payment and profitability uncertainty for hospitals and device makers.
  • Cost and compatibility concerns: Single-use disposal of the system and compatibility limited to .014" guidewires may increase per-procedure costs and restrict the device's applicability in peripheral vascular procedures, impacting hospital procurement decisions and device adoption.

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