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NeoGenomics, Inc. (NEO) SEC Filings & Earnings Calls

EquiReason read 19 NeoGenomics, Inc. SEC filings in the last 12 months. Latest: 8-K on 2026-10-05 — NeoGenomics announces CEO succession: Warren Stone (COO) to become CEO effective Jan 4, 2027; Tony Zook becomes Executive Chair; preliminary Q3 revenue ~$209M with NGS growth ~28%;.

Source: SEC EDGAR filings · figures as of 2026-06-30 · read by EquiReason

NEONeoGenomics, Inc.Follow NEO — free
Diagnostics & Research · Healthcare
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Every filing, read

last 12 months · SEC

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5 Oct 20268-K · 2.02, 5.02, 5.03NeoGenomics announces CEO succession: Warren Stone (COO) to become CEO effective Jan 4, 2027; Tony Zook becomes Executive Chair; preliminary Q3 revenue ~$209M with NGS growth ~28%; full-year revenue guidance expected to increase at midpointopen

Figures in the filing · each found in the filing text

Revenue · Q3-2026$209M
NGS revenue growth · NGS · Q3-202628.0%

Guidance

Full year total revenue guidance expected to increase at midpoint resulting from third quarter performance

Full-year revenue guidance expected to increase at midpoint due to Q3 performance.

Risks flagged

CEO transition could cause short-term uncertainty, but planned succession mitigates risk.

“Planned succession with internal promotion.”
Read the original on SEC EDGAR ↗
11 Aug 20268-K · 5.02Reported a director or officer change (departure, election, appointment or pay arrangement)open

Risks flagged

Key executive departure may create transitional risk in legal and business development functions.

“EVP, General Counsel & Business Development departing; separation payments triggered.”
Read the original on SEC EDGAR ↗
28 Jul 20268-K · 2.02Q2 2026 total revenue +11% YoY to $202M; clinical revenue +14%, NGS +26%; GAAP net income $2M vs loss; adjusted EBITDA +36% to $14M; FY2026 guidance raised for revenue and adjusted EBITDA.earningsopen

Figures in the filing · each found in the filing text

Total Revenue · Q2-2026$202M+11% y/y
Clinical Revenue · Q2-2026$187M+14% y/y
NGS Revenue Growth · Q2-202626.0%
GAAP Net Income · Q2-2026$2M
Adjusted EBITDA · Q2-2026$14M+36% y/y
Adjusted Gross Profit Margin · Q2-202648.0%
Cash and Cash Equivalents · Q2-2026$146M
Operating Cash Flow · Q2-2026$20M
Average Revenue per Clinical Test · Q2-2026$515.00+12% y/y
Clinical Volume Growth · Q2-20262.0%

Guidance

FY2026 revenue raised to $802-806M from $797-803M; adjusted EBITDA raised to $56-58M from $55-57M; net loss improved to $(42)-$(34)M from $(63)-$(50)M

Revenue and adjusted EBITDA guidance raised; net loss guidance improved; strong execution and mix shift.

Risks flagged

DOJ civil settlement finalized; consulting services investigation resolved.

“Finalized a civil settlement with the Department of Justice resolving a self-disclosed matter and investigation concerning consulting services provided by the Company.” · word for word

Convertible debt adds leverage; $316M notes due 2032 at 0.75%.

“completion of a $316 million private offering of 0.75% convertible senior notes due 2032” · word for word
Read the original on SEC EDGAR ↗
28 Jul 202610-QNeoGenomics reported Q2 2026 revenue growth of 11.2% YoY, gross margin expansion to 45.6%, and a return to profitability with net income of $2.2M.earningsopen

Figures in the filing · each found in the filing text

Revenue · Q2-2026$202M+11% y/y
Gross Profit Margin · Q2-202645.6%
Adjusted EBITDA · Q2-2026$14M+36% y/y
Net Income (Loss) · Q2-2026$2M
Cash and Cash Equivalents · 2026-06-30$146M
Operating Cash Flow · H1-2026$12M

Risks flagged

Pharmaceutical Clinical Trial Slowdown

“lower non-clinical revenue due to macro clinical trial trends in the pharmaceutical industry” · word for word

Regulatory Risk for LDTs

“future legislative, regulatory, or administrative actions could reintroduce FDA oversight of certain LDTs, which could increase compliance obligations and costs” · word for word

Tariff Impact

“We may experience increased supply chain challenges and customer demand uncertainty due to rapid changes in global trade policies” · word for word
Read the original on SEC EDGAR ↗
20 Jul 20268-K · 7.01, 8.01DOJ settlement payment $10M; Accrued reserve for investigation $11Mopen

Figures in the filing · each found in the filing text

DOJ settlement payment · consolidated · 2026-06-20$10M
Accrued reserve for investigation · consolidated · Q1-2026$11M

Risks flagged

Legal overhang resolved; settlement amount below accrued reserve, indicating no additional financial hit.

“Settlement $9.8M vs reserve $11.2M; no admission of liability.”
Read the original on SEC EDGAR ↗
25 Jun 20268-K · 5.02, 7.01NeoGenomics appointed Carolyn S. Starrett to its Board of Directors, increasing board size from nine to ten. Ms. Starrett brings experience in AI and data insights in cancer care.SEC ↗
22 Jun 20268-K · 1.01, 2.03, 3.02, 8.01NeoGenomics issued $276M aggregate principal of 0.75% convertible senior notes due 2032, repurchased $276M of existing 0.25% notes for ~$263.19M, and repurchased up to $25M of common stock at $10.49/share.open

Risks flagged

Dilution risk if stock price exceeds conversion price; capped calls provide partial offset.

“Conversion price $14.16, cap price $20.98; capped calls cost $28.7M.”
Read the original on SEC EDGAR ↗
17 Jun 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen

Risks flagged

Potential dilution from future conversion of notes.

“Offering of convertible notes implies potential equity dilution.”
Read the original on SEC EDGAR ↗
15 Jun 20268-K · 8.01Disclosed a material event under other events (litigation, recall, contract loss, or major announcement); filed financial statements and exhibits with this reportopen

Risks flagged

Potential dilution from future conversion.

“Proposed convertible notes offering.”
Read the original on SEC EDGAR ↗
22 May 20268-K · 5.02, 5.07Reported the departure of a director or principal officer (CEO/CFO change); submitted matters to a vote of security holdersopen

Risks flagged

Potential dilution from future equity grants under the amended plan.

“5,000,000 additional shares authorized.”
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28 Apr 20268-K · 2.02Consolidated revenue $187M (+11% y/y); Net loss $-17M (+34% y/y); Adjusted EBITDA $9M (+27% y/y); Guidance: Revenue guidance raised from $793-801M to $797-803Mearningsopen

Figures in the filing · each found in the filing text

Consolidated revenue · Q1-2026$187M+11% y/y
Net loss · Q1-2026$-17M+34% y/y
Adjusted EBITDA · Q1-2026$9M+27% y/y
Average revenue per clinical test · Clinical · Q1-2026$495.00+8% y/y
Cash and cash equivalents and marketable securities · Q1-2026$146M
FY2026 revenue guidance (low) · FY2026$797M+10% y/y
FY2026 revenue guidance (high) · FY2026$803M+10% y/y

Guidance

Revenue guidance raised from $793-801M to $797-803M

Raised FY2026 revenue guidance reflecting strong Q1 performance and new product momentum; margin improving; demand accelerating.

Risks flagged

Dependence on reimbursement coverage for new tests; MolDX decision is favorable but limited to PanTracer LBx.

“Announced a favorable MolDX coverage decision for PanTracer™ LBx” · word for word

Competitive market for MRD testing; RaDaR ST faces established competitors.

“Launched RaDaR® ST, a circulating tumor DNA (ctDNA) assay for detecting molecular residual disease (MRD), which we estimate represents a $20 billion addressable market, growing at 30% annually, which we believe is less than 10% penetrated.” · word for word
Read the original on SEC EDGAR ↗
28 Apr 202610-QRevenue $187M (+11% y/y); Gross Profit Margin 43.3; Net Loss $-17M (+34% y/y); Guidance: Capex guided $30M-$35M for FY2026open

Figures in the filing · each found in the filing text

Revenue · Q1-2026$187M+11% y/y
Gross Profit Margin · Q1-202643.3%
Net Loss · Q1-2026$-17M+34% y/y
Adjusted EBITDA · Q1-2026$9M+27% y/y
Operating Cash Flow · Q1-2026$-8M+68% y/y
Cash and Cash Equivalents · Q1-2026$146M-58% y/y
Capital Expenditures · Q1-2026$5M

Guidance

Capex guided $30M-$35M for FY2026

Management reaffirms focus on sustainable growth, innovation in MRD and therapy selection, and operational efficiency. Capex guidance of $30M-$35M for FY2026 implies continued investment.

Risks flagged

LDT Regulation Uncertainty

“Notwithstanding the court’s decision, future legislative, regulatory, or administrative actions could reintroduce FDA oversight of certain LDTs, which could increase compliance obligations and costs.” · word for word

Tariff Impact on Supply Chain

“We may experience increased supply chain challenges and customer demand uncertainty due to rapid changes in global trade policies, which may impact our net sales and profitability.” · word for word
Read the original on SEC EDGAR ↗
6 Apr 2026DEF 14AProxy statement for 2026 annual meeting; includes say-on-pay, equity plan amendment, and director elections.open

Figures in the filing · each found in the filing text

Revenue · FY2025$727M+10% y/y
Adjusted EBITDA · FY2025$43M+10% y/y
NGS Testing Revenue Growth · FY202522.0%
Adjusted Gross Profit Growth · FY20257.5%
Say-on-Pay Support · 202581.8%
CEO Base Salary · 2025$850000.00
CEO Target Bonus Percentage · 2025100.0%
CEO Equity Target · 2025$8M
Equity Plan Share Increase Requested · 20265,000,000
Burn Rate · FY20253.3%

Risks flagged

CEO transition risk

“CEO transition following the decision by our then CEO, Mr. Smith, to retire effective April 1, 2025.” · word for word

Stockholder compensation concerns

“In 2025, we received 81.77% support for our annual say-on-pay proposal.” · word for word

Equity dilution risk

“increase the number of shares of common stock reserved for issuance under the 2023 Equity Incentive Plan by 5,000,000 shares to 13,300,000 shares.” · word for word
Read the original on SEC EDGAR ↗
17 Feb 20268-K · 2.02Consolidated revenue $727M (+10% y/y); Net loss $-108M (+37% y/y); Adjusted EBITDA $43M (+9% y/y); Guidance: FY2026 revenue $793-801M (9-10% YoY), adjusted EBITDA $55-57M (27-31% YoY), net loss $(63)-$(50)M.earningsopen

Figures in the filing · each found in the filing text

Consolidated revenue · FY2025$727M+10% y/y
Net loss · FY2025$-108M+37% y/y
Adjusted EBITDA · FY2025$43M+9% y/y
Cash and cash equivalents · Q4-2025$160M
Average revenue per clinical test · clinical · Q4-2025$488.00+5% y/y
NGS growth · NGS · Q4-202523.0%

Guidance

FY2026 revenue $793-801M (9-10% YoY), adjusted EBITDA $55-57M (27-31% YoY), net loss $(63)-$(50)M.

FY2026 guidance raised: revenue growth 9-10%, adjusted EBITDA growth 27-31%, net loss narrowing significantly.

Risks flagged

Net loss increased 37% in FY2025 to $108M, though expected to narrow in FY2026.

“Full year net loss increased 37% to $108 million” · word for word

Non-clinical revenue impacted by macro trends in pharma/biotech.

“lower non-clinical revenue due to macro trends in the pharmaceutical and biotech industries” · word for word
Read the original on SEC EDGAR ↗
17 Feb 202610-KRevenue $727M (+10% y/y); Net Loss $-108M; Adjusted EBITDA $43M (+10% y/y); Guidance: Capex guided $30M-$35M for 2026open

Figures in the filing · each found in the filing text

Revenue · FY2025$727M+10% y/y
Net Loss · FY2025$-108M
Adjusted EBITDA · FY2025$43M+10% y/y
Gross Profit Margin · FY202543.2%
Cash and Cash Equivalents · 2025-12-31$160M-57% y/y
Capital Expenditures · FY2025$27M
Client Direct Billing % of Revenue · FY202571.0%
Commercial Insurance % of Revenue · FY202516.0%
Medicare and Other Government % of Revenue · FY202513.0%
Impairment Charges · FY2025$28M

Guidance

Capex guided $30M-$35M for 2026

Management expects continued growth through innovation in MRD and therapy selection, community channel expansion, and operational efficiency. Capex guided higher.

Risks flagged

Regulatory Risk - LDT Oversight

“On March 31, 2025, the U.S. District Court for the Eastern District of Texas vacated the FDA's final rule in its entirety... future legislative, regulatory, or administrative actions could reintroduce FDA oversight of certain LDTs, which could increase compliance obligations and costs.” · word for word

Impairment Risk on Acquired Assets

“Impairment charges consisted of an $11.4 million impairment on InVisionFirst®-Lung intangible assets, $15.9 million impairment on the disposal of substantially all of Trapelo's assets.” · word for word

Cash Burn / Liquidity Risk

“Cash and cash equivalents, end of year $159,618, down from $367,012 at beginning of year, primarily due to repayment of $201.3M convertible notes.” · word for word
Read the original on SEC EDGAR ↗
12 Jan 20268-K · 2.02, 5.02NeoGenomics announces preliminary Q4/FY2025 revenue (~$190M Q4, ~$727M FY) and CFO transition: Jeff Sherman retiring, Abhishek Jain appointed as EVP Finance, to become CFO on March 2, 2026.open

Figures in the filing · each found in the filing text

revenue · Q4-2025$190M+11% y/y
revenue · FY2025$727M+10% y/y

Risks flagged

Preliminary results are unaudited and subject to change, which may be material.

“The selected financial results are based on preliminary unaudited information and management estimates, are not a comprehensive statement of the Company’s financial results ... and are subject to change. Such changes may be material.” · word for word
Read the original on SEC EDGAR ↗
30 Dec 20258-K · 5.02Reported the departure of a director or principal officer (CEO/CFO change); filed financial statements and exhibits with this reportSEC ↗
28 Oct 20258-K · 2.02NeoGenomics reports Q3 2025 revenue up 12% YoY to $188M, clinical revenue up 18%, NGS up 24%, reaffirms FY2025 guidance; net loss widens to $27M, adjusted EBITDA down 9% to $12.2M.earningsopen

Figures in the filing · each found in the filing text

Consolidated revenue · Q3-2025$188M+12% y/y
Clinical revenue growth · Clinical · Q3-202518.0%
NGS revenue growth · Clinical · Q3-202524.0%
Net loss · Q3-2025$-27M+53% y/y
Adjusted EBITDA · Q3-2025$12M-9% y/y
Cash and cash equivalents and marketable securities · Q3-2025$164M
Average revenue per clinical test · Clinical · Q3-2025$476.00+3% y/y

Guidance

FY2025 revenue $720-726M; net loss $(116)-$(108)M; adjusted EBITDA $41-44M

Full-year guidance reaffirmed; management optimistic about clinical growth and NGS momentum.

Risks flagged

Non-clinical revenue weakness persists, but anticipated and incorporated in guidance.

“Continued weakness in non-clinical revenue, which we anticipated and incorporated into the full-year guidance.” · word for word

Impairment charge from Trapelo sale indicates potential asset write-downs.

“$7.1 million of impairment charges from impairment of assets held for sale related to the planned sale of Trapelo.” · word for word
Read the original on SEC EDGAR ↗
28 Oct 202510-QQ3 2025 revenue grew 11.9% YoY; net loss widened to $27.1M due to impairment charges; Adjusted EBITDA declined slightly to $12.2M.earningsopen

Figures in the filing · each found in the filing text

Revenue · Q3-2025$188M+12% y/y
Revenue · 9M-2025$537M+10% y/y
Gross Profit Margin · Q3-202542.8%
Gross Profit Margin · 9M-202543.0%
Net Loss · Q3-2025$-27M
Net Loss · 9M-2025$-98M
Adjusted EBITDA · Q3-2025$12M-9% y/y
Adjusted EBITDA · 9M-2025$30M+8% y/y
Cash and Equivalents · Q3-2025$164M
Operating Cash Flow · 9M-2025$4M

Guidance

Capex guidance $30M-$35M for FY2025

Revenue growth driven by volume and mix; gross margin under pressure from costs; capex guidance maintained; no explicit revenue or EBITDA guidance.

Risks flagged

Impairment risk from InVisionFirst-Lung and disposal group

“Impairment charges consisted of an $11.4 million impairment on InVisionFirst®-Lung intangible assets, a $15.3 million impairment on the disposal group held for sale, and a $0.4 million loss on InVisionFirst®-Lung inventory write-off.” · word for word

Tariff and trade policy risk

“In addition, we are monitoring the effects of recently implemented tariffs and the potential imposition of modified or additional tariffs. We may experience increased supply chain challenges and customer demand uncertainty due to rapid changes in global trade policies, which may impact our net sales and profitability.” · word for word

Clinical trial revenue slowdown

“Revenues from the Pathline acquisition also contributed to revenue growth, which was partially offset by lower non-clinical revenue due to macro clinical trial trends in the pharmaceutical industry, and a less favorable test mix.” · word for word

Cash burn from convertible note repayment

“This change was primarily due to $201.3 million cash used for the repayment of the convertible senior notes.” · word for word
Read the original on SEC EDGAR ↗

NeoGenomics, Inc. — questions

What did NeoGenomics, Inc. file recently?
19 SEC filings in the last 12 months. Latest: 8-K on 2026-10-05 — NeoGenomics announces CEO succession: Warren Stone (COO) to become CEO effective Jan 4, 2027; Tony Zook becomes Executive Chair; preliminary Q3 revenue ~$209M with NGS growth ~28%; full-year revenue guidance expected to increase at midpoint

Every figure on this page comes from NeoGenomics, Inc.'s own SEC filings — see them on SEC EDGAR. Price data is licensed and shown only inside the product.

How these figures are read: methodology · EquiReason.