Analyst Ratings February 11, 2026

Stifel Sticks With Buy on Glaukos, Sees Nearly 50% Upside to $160 Target

Analyst survey finds encouraging iDose adoption despite LCD risks; preliminary Q4 2025 revenue and an FDA label change add to bullish case

By Caleb Monroe GKOS
Stifel Sticks With Buy on Glaukos, Sees Nearly 50% Upside to $160 Target
GKOS

Stifel has reconfirmed a Buy rating and set a $160 price target on Glaukos Corporation (GKOS), citing an attractive risk-reward for the company’s iDose franchise even as potential Local Coverage Determination - LCD - restrictions loom. The firm’s assessment rests on survey work, early commercial checks, and recent company disclosures including preliminary fourth-quarter 2025 revenue and an FDA labeling supplement for iDose TR. Short-term profitability remains negative, but revenue momentum and anticipated 2027 growth tied to Epioxa underpin Stifel’s stance.

Key Points

  • Stifel reaffirms Buy rating and sets a $160 price target on Glaukos, implying nearly 50% upside from the cited $107.09 share price; shares are trading above Fair Value according to InvestingPro.
  • Survey work and commercial checks indicate growing iDose utilization among commercial and Medicare Advantage patients, supporting Stifel’s expectation of modest 2026 tailwinds and larger 2027 impact tied to Epioxa.
  • Glaukos reported strong revenue momentum - preliminary Q4 2025 revenue of $143 million, up 36% YoY - and received FDA approval for an iDose TR labeling supplement that permits re-administration for patients with a healthy cornea.

Stifel has reiterated a Buy recommendation and raised its price target on Glaukos Corporation to $160, maintaining that the upside on the stock remains compelling despite regulatory and coverage uncertainties. At the time referenced by analysts, the share price was $107.09, which Stifel says implies nearly 50% upside to the $160 target. Separate market data noted that the shares are trading above their Fair Value.

Survey work and LCD considerations

The research team surveyed 30 respondents to gauge near-term catalysts for iDose and to quantify the potential impact of Local Coverage Determination - LCD - limitations. Respondents signaled that combination utilization restrictions represent a meaningful LCD risk. The survey also revealed higher-than-anticipated combination iDose procedures, but Stifel’s scenario modeling concluded the aggregate risk-reward profile remains favorable.

Commercial checks and timing of adoption

Stifel’s channel checks flagged encouraging early signs that iDose utilization could expand among commercial and Medicare Advantage patient cohorts. Based on those checks, the firm said it is increasingly confident these payer segments will contribute at least a small incremental lift for iDose in 2026, with a more material effect expected in 2027.

Additional January checks across 55 respondents supported the bullish view, showing stronger-than-expected first-quarter 2026 volume expectations and robust re-administration estimates under the newly approved label for iDose TR.

Financial backdrop and upcoming catalyst

While Stifel points to growth opportunities, company-level profitability remains a limitation in the near term. Data covering the last twelve months show Glaukos produced a diluted EPS of -$1.54. At the same time, Glaukos reported robust top-line momentum, with revenue growth of 30.38% over the same trailing twelve-month period.

Investors will have a nearer-term opportunity to reassess company results and iDose trends when Glaukos releases quarterly results on February 17.

Preliminary fourth-quarter 2025 results and label expansion

Glaukos announced preliminary fourth-quarter 2025 revenue of $143 million, representing a 36% year-over-year increase and coming in about 10% above analyst expectations. U.S. glaucoma sales were reported at $86 million, roughly 5% higher than consensus forecasts, while iDose revenue was disclosed at $45 million, in line with expectations. International glaucoma sales were approximately $33 million, about 6% above the expected $31 million.

Regulatory developments also contributed to the recent outlook. The U.S. Food and Drug Administration approved a labeling supplement for iDose TR that allows re-administration in patients with a healthy cornea, expanding potential treatment flexibility for clinicians managing glaucoma over the long term.

Analyst and market reactions

Following these developments, another firm, BTIG, increased its price target for Glaukos to $131 and maintained a Buy rating. Stifel reiterated its Buy stance and reiterated the $160 target, attributing the raise to positive survey evidence around Epioxa and projecting an "Epioxa-driven 2027+ growth acceleration story." Stifel described itself as "strong buyers" of the shares.

Balance sheet and additional resources

Stifel highlighted Glaukos’s liquidity position, noting a current ratio of 5.2, which indicates liquid assets substantially exceed short-term obligations. For readers seeking deeper financial detail, the analysis referenced access to expanded financial health metrics and additional ProTips available through InvestingPro, including a full Pro Research Report and nine supplemental ProTips.


Overall, Stifel’s view balances the revenue momentum and regulatory advances with LCD and profitability considerations, leaving the firm constructive on Glaukos as it heads into upcoming public disclosures and expected commercial expansion for iDose and Epioxa into 2027.

Risks

  • Potential LCD-imposed restrictions - particularly limits on combination procedures - represent a meaningful coverage risk that could constrain iDose utilization and revenue growth; this affects the medical device and healthcare services sectors.
  • Glaukos is not profitable on a trailing twelve-month basis, with a diluted EPS of -$1.54, which poses execution and capital-allocation risk for investors focused on near-term earnings; this impacts equity investors and healthcare-focused funds.
  • Survey responses showed higher-than-anticipated combination iDose procedures, which could complicate reimbursement dynamics and payer responses; this creates uncertainty for commercial adoption projections across payer-managed care segments.

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