GTHPOTCElectromedical & Electrotherapeutic ApparatusUS GAAP · USD

Guided Therapeutics Inc

Guided Therapeutics Inc. develops and commercializes the LuViva Advanced Cervical Scan, an electromedical device used for cervical cancer screening. The company’s business is centered on selling LuViva instruments and disposables through direct and distribution channels, while it continues to pursue regulatory approvals needed to expand commercial adoption.

Revenue0.8m USD
+10,857.1 %y/y
Operating profit (EBIT)-2.4m USD
−12.5 %y/y
EBIT margin-309.3%
+29,805.0 ppy/y
Net income-3.2m USD
−32.2 %y/y
Free cash flow-1.1m USD

Fiscal year 2025 · change from previous year

Development 2020–2025

-4-3-2-101m USD2020: 0.10 m USD2020: EBIT -1.1 m USD20202021: 0.08 m USD2021: EBIT -2.4 m USD20212022: 0.01 m USD2022: EBIT -3.3 m USD20222023: 0.10 m USD2023: EBIT -3.5 m USD20232024: 0.01 m USD2024: EBIT -2.1 m USD20242025: 0.77 m USD2025: EBIT -2.4 m USD20250.77-2.4
RevenueOperating profit (EBIT)

Business

Share of revenue
LuViva devices70 %

Cervical cancer screening instruments sold as instrumentation packages to hospitals, clinics, and partners.

Disposables and consumables30 %

RFID chips and related consumable components used with LuViva systems.

Customers

The company sells primarily to medical distributors, healthcare systems, hospitals, and clinics that use LuViva for cervical cancer screening. It is also pursuing government and public-health buyers, including the Turkish Ministry of Health, because large-scale screening programs can create recurring demand for devices and disposables.

Medical distributors

Buy LuViva systems for resale and market development in approved territories.

Hospitals and clinics

Purchase devices for cervical cancer screening programs and patient throughput.

Government health ministries

Evaluate LuViva for public screening programs where scale and cost matter.

Government hospital systems

Buy devices for regional deployment, such as the Sulawesi hospital system in Indonesia.

Strategy

The company’s near-term strategy is to secure regulatory approvals, convert distributor relationships into shipments, and fund operations until commercialization scales. It is also trying to reduce execution risk by using external financial support, advance payments, and partner-led market entry rather than building a large direct-sales footprint too early.

Regulatory approvals in the U.S. and ChinaShort term

Commercial scale depends on FDA and NMPA clearance, especially for the largest target markets.

Distributor-led international expansionMedium term

The company lacks a large direct sales infrastructure, so partners are essential for market access.

Cash preservation and external fundingShort term

The business remains loss-making and needs capital to continue operations and commercialization.

Geography

Guided Therapeutics is still a small-revenue company, but its commercial focus spans the United States, China, and Europe, with additional activity in Turkey and Indonesia. Geography matters because sales depend heavily on local regulatory approvals, distributor execution, and the timing of market access in each country.

Risks

Guided Therapeutics faces substantial regulatory, funding, and commercialization risk because its revenue base is still small and dependent on approvals that can be delayed or denied. The company also has concentration risk in a few markets and counterparties, while medical-device adoption depends on clinical acceptance, distributor performance, and manufacturing execution.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Regulatory approval delays2Geopolitical and country-specific market risk5
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 / financing riskImpact: Critical

    The company has recurring losses and needs additional capital to continue operations and fund studies.

    ExposureOperationsClinical workManufacturing readiness
  2. Regulatory approval delaysImpact: HighLikelihood: High

    Sales depend on FDA and NMPA clearance, and delays directly push out revenue and cash generation.

    Exposure: LuViva commercialization in the U.S. and China

  3. Distributor and counterparty riskImpact: High

    Sales depend on partners such as SMI, Newmars, and HDMT, and one partner is in contractual default.

    ExposureOrder conversionCollectionsMarket access
  4. Market acceptance riskImpact: High

    The product must gain clinical and commercial acceptance versus existing cervical screening methods.

    ExposureAdoption by hospitalsClinicsPublic health systems
  5. Geopolitical and country-specific market riskImpact: MediumLikelihood: High

    Russia and other markets may face approval, trade, or operating constraints.

    Exposure: European distribution and international expansion

Accounting

Judgemental items
Revenue recognition timing

Some customer payments are recorded as deferred revenue until shipment or approval conditions are met.

Impact: Can shift revenue between quarters and affect comparability.

Deferred revenue

The company reported a sizable deferred revenue balance tied to future shipments.

Impact: Indicates revenue already billed or collected but not yet recognized.

Inventory valuation

Devices and components must be written down if demand or approval timing changes.

Impact: Can affect gross margin and operating results.

Fair value of equity instruments

Employee, service-provider, and investor instruments are valued using option-pricing models.

Impact: Can create non-cash expense volatility.

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026

Guided Therapeutics Inc (OTC) – Electromedical & Electrotherapeutic Appa | Financial Analysis – Clarifo