GCTKNasdaqSurgical & Medical Instruments & ApparatusUS GAAP · USD

Glucotrack, Inc.

Glucotrack, Inc. is a U.S.-based medical device developer focused on novel diabetes technologies. Its core program is the Glucotrack CBGM, an implantable continuous blood glucose monitor being developed for people with Type 1 diabetes and insulin-dependent Type 2 diabetes.

Operating profit (EBIT)-16.1m USD
−10.6 %y/y
Net income-19.4m USD
+14.2 %y/y
Free cash flow-15.3m USD
−21.8 %y/y

Fiscal year 2025 · change from previous year

Development 2020–2025

-20-15-10-50m USD2020: EBIT -3.1 m USD20202021: EBIT -4.0 m USD20212022: EBIT -4.4 m USD20222023: EBIT -7.1 m USD20232024: EBIT -15 m USD20242025: EBIT -16 m USD2025-16
RevenueOperating profit (EBIT)

Business

Share of revenue
Implantable glucose monitoring devices0 %

The Glucotrack CBGM and related implantable continuous blood glucose monitoring technology for diabetes care.

Clinical development services0 %

Clinical trial execution, testing, and development activities needed to advance the device toward commercialization.

Regulatory and FDA readiness0 %

Work supporting FDA registration, documentation, and product approval preparation.

R&D and product engineering100 %

Internal research, design, and engineering for new CBGM models and product candidates.

Customers

Glucotrack does not yet appear to have commercial customers because the CBGM has not been commercialized. Its eventual buyers are expected to be people with diabetes, especially Type 1 patients and insulin-dependent Type 2 patients, likely through healthcare providers and reimbursement channels. The company’s near-term stakeholders are clinical investigators, regulators, and financing partners that support development.

Type 1 diabetes patients

Future end users of the implantable CBGM who need continuous glucose data for insulin management.

Insulin-dependent Type 2 diabetes patients

Future end users who may benefit from continuous monitoring to improve glycemic control.

Clinical and regulatory stakeholders

Hospitals, investigators, and regulators involved in trials, validation, and FDA registration.

Capital providers

Equity and debt investors funding development before commercialization.

Strategy

The company’s strategy is to advance the Glucotrack CBGM through clinical development, FDA registration, and eventual commercialization. Near term, management is focused on preserving liquidity, raising capital, and funding the next stages of development while expanding clinical trial activity and product iterations.

Clinical development of Glucotrack CBGMShort term

Clinical evidence is required to support regulatory approval and future adoption.

FDA registration and regulatory progressShort term

Regulatory clearance is the gate to commercialization and revenue generation.

Capital raising and liquidity preservationShort term

The company is a going concern and needs external funding to continue operations.

Geography

Glucotrack is headquartered in the United States and its filings are on a U.S. reporting basis. The business currently appears centered on U.S.-based R&D, clinical, and regulatory work, with no disclosed commercial geographic revenue mix because the product has not been commercialized. Geography matters mainly through U.S. FDA oversight, domestic financing access, and the location of clinical development activities.

Risks

Glucotrack faces classic pre-commercial medtech risks: it has not yet generated product revenue, needs significant additional funding, and depends on successful clinical and regulatory execution. The company also disclosed substantial doubt about its ability to continue as a going concern, making financing availability a central business risk.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Going concern and liquidity shortfall1Clinical and regulatory execution risk2Financing and dilution risk3Commercial adoption risk4
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Going concern and liquidity shortfallImpact: CriticalLikelihood: High

    The company states current cash is not sufficient for the next twelve months and it needs external financing.

    ExposureOperationsClinical trialsProduct development
  2. Clinical and regulatory execution riskImpact: HighLikelihood: High

    Commercialization depends on successful trials and FDA registration, both of which can be delayed or fail.

    Exposure: Glucotrack CBGM development timeline

  3. Financing and dilution riskImpact: HighLikelihood: High

    The company plans to fund operations through debt or equity, which may be unavailable or dilutive.

    Exposure: Shareholders and capital structure

  4. Commercial adoption riskImpact: MediumLikelihood: High

    Even after approval, the implantable device must win physician and patient acceptance versus existing monitoring options.

    Exposure: Future revenue conversion

Accounting

Judgemental items
Derivative liabilities fair value

The company says other income/expense includes changes in fair value of derivative liabilities, which can create volatility.

Impact: Can materially swing quarterly net loss

Stock-based compensation

Personnel-related expenses in R&D and G&A include stock-based compensation, affecting operating expense levels.

Impact: Raises reported operating costs without cash outflow

Going concern estimates

Management must assess whether available cash is sufficient and disclose substantial doubt when it is not.

Impact: Affects financial statement presentation and investor risk assessment

Convertible notes and warrant accounting

Recent financing activity includes convertible notes and warrant exchanges, which can require complex classification and valuation judgments.

Impact: Can affect equity, liabilities, and financing expense

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026