Logotype for Monogram Technologies Inc

Monogram Technologies (MGRM) Q3 2024 earnings summary

Event summary combining transcript, slides, and related documents.

Logotype for Monogram Technologies Inc

Q3 2024 earnings summary

13 Jan, 2026

Executive summary

  • Ended Q3 2024 with $16.6 million in cash and a $1.2 million monthly cash run rate, supported by a $13 million Series D Preferred Stock offering and $4.3 million from an at-the-market equity program.

  • Focused on commercializing a fully autonomous saw-cutting robot for orthopedic surgery, with all employees dedicated to R&D and regulatory milestones.

  • Submitted first 510(k) application to the FDA in July 2024, received an Additional Information Request in September, and prepared a detailed response for a December Q-Sub meeting.

  • No product revenue recognized for the nine months ended September 30, 2024, as commercialization is pending regulatory approvals.

  • Anticipates significant milestones in 2025–2026, including potential product launch and expansion into international markets.

Financial highlights

  • Net loss for Q3 2024 was $5.0 million, with a year-to-date net loss of $12.1 million, and operating expenses for Q3 2024 rose 37% year-over-year to $5.1 million.

  • Operating cash flow year-to-date is $10.9 million, with no traditional debt and minimal short-term warrant obligations.

  • Cash and cash equivalents were $16.6 million as of September 30, 2024, up from $13.6 million at year-end 2023.

  • Total stockholders' equity increased to $17.4 million from $13.4 million at December 31, 2023.

  • No revenue was reported for the three or nine months ended September 30, 2024.

Outlook and guidance

  • Management believes current cash balances and available capital under equity programs are sufficient to meet near-term capital needs and support operations for at least 12 months.

  • Confident in meeting short-term milestones with current funding; potential to accelerate development if additional capital or strategic partnerships are secured.

  • OUS clinical trial in India expected to begin in 2025, with live patient surgeries anticipated next year.

  • FDA clearance decision expected by Q2 2025 if the full review period is used; commercialization could begin in 2025 or 2026 depending on regulatory outcomes.

  • Plans to expand into other large international markets, including Indonesia, South America, and the Middle East.

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