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Final 2026 Clinical Lab Fee Schedule Indicates a 47% Increase in Payment Determination for the Category I CPT Code for OGM use in Hematologic Malignancies

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Bionano Laboratories (Nasdaq: BNGO) announced that the 2026 Clinical Lab Fee Schedule posted by CMS increases the Category I CPT code 81195 payment by 47%, from $1,263.53 to $1,853.22, effective January 1, 2026.

The CDLT committee voted 10-0 in favor of the proposed crosswalk that supported the higher payment; CMS adopted the panel recommendation. CPT code 81195 covers OGM use in cytogenomic analysis for hematologic malignancies. Bionano said the new payment level should aid reimbursement for its OGM-based LDTs such as OGM-Dx HemeOne.

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Positive

  • Payment increase of 47% for CPT 81195
  • New rate set at $1,853.22 effective Jan 1, 2026
  • CDLT vote unanimous 10-0 supporting the crosswalk
  • CPT recognition strengthens reimbursement pathway for OGM LDTs

Negative

  • None.

News Market Reaction – BNGO

+2.98%
1 alert
+2.98% News Effect
+$509K Valuation Impact
$18M Market Cap
0.0x Rel. Volume

On the day this news was published, BNGO gained 2.98%, reflecting a moderate positive market reaction. This price movement added approximately $509K to the company's valuation, bringing the market cap to $18M at that time.

Data tracked by StockTitan Argus on the day of publication.

Key Figures

CPT 81195 increase: 47% Original payment: $1,263.53 New payment: $1,853.22 +5 more
8 metrics
CPT 81195 increase 47% Change in CLFS payment determination for 2026
Original payment $1,263.53 CPT 81195 CLFS payment effective January 1, 2025
New payment $1,853.22 Re-priced CPT 81195 CLFS payment effective January 1, 2026
CDLT vote 10-0 Committee vote in favor of higher payment crosswalk
Effective date (original) January 1, 2025 Initial CLFS payment determination for CPT 81195
Effective date (re-price) January 1, 2026 CLFS re-pricing date for CPT 81195
CPT codes count 2 codes OGM-related Category I CPT codes: 81195 and 81354
CPT code 81195 OGM in cytogenomic genome-wide analysis for hematologic malignancies

Market Reality Check

Price: $1.12 Vol: Volume 173,800 is below 2...
low vol
$1.12 Last Close
Volume Volume 173,800 is below 20-day average 291,876 (relative volume 0.6x), suggesting limited pre-news positioning. low
Technical Shares at $1.66 are trading below the 200-day MA of $3.05 and remain 92.72% under the 52-week high of $22.80.

Peers on Argus

Peers showed mixed moves: HBIO -4.23%, NXGL +13.58%, RVP +2.44%, FEMY +0.60%, MH...

Peers showed mixed moves: HBIO -4.23%, NXGL +13.58%, RVP +2.44%, FEMY +0.60%, MHUA -27.18%. The lack of a consistent direction points to this CPT-pricing news being stock-specific rather than a coordinated sector rotation.

Historical Context

5 past events · Latest: Dec 03 (Positive)
Pattern 5 events
Date Event Sentiment Move Catalyst
Dec 03 Reimbursement update Positive +3.0% CMS raised CPT 81195 payment 47%, improving OGM reimbursement outlook.
Nov 13 Earnings results Positive -8.1% Q3 2025 revenue grew 21% YoY with higher gross margin and lower opex.
Nov 06 Clinical study data Positive -4.7% MD Anderson study showed OGM can overcome limitations of targeted RNA‑seq.
Oct 30 Earnings preview Neutral -1.6% Announcement of date and webcast details for Q3 2025 earnings call.
Oct 23 Conference highlights Positive -0.5% ASHG presentations underscored expanding use of OGM in genetic disease.
Pattern Detected

Across recent events, BNGO often saw negative price reactions to positive news, with 3 of 4 clearly positive items followed by declines; today’s reimbursement uplift was one of the few aligned positive reactions.

Recent Company History

Over the last few months, Bionano reported Q3 2025 revenue of $7.4M, up from $6.1M, along with cost cuts and a narrower loss. Scientific updates highlighted optical genome mapping (OGM) advantages in acute leukemia and broad rare-disease applications. Despite generally positive operational and scientific news, shares often traded lower afterward. Today’s CLFS decision, lifting CPT code 81195 payment to $1,853.22 from $1,263.53 effective January 1, 2026, directly supports reimbursement for OGM-based LDTs, tying regulatory reimbursement progress to Bionano’s existing test menu.

Market Pulse Summary

This announcement centers on CMS’s final 2026 CLFS decision to raise payment for Category I CPT code...
Analysis

This announcement centers on CMS’s final 2026 CLFS decision to raise payment for Category I CPT code 81195 by 47%, from $1,263.53 to $1,853.22 effective January 1, 2026. The higher rate supports reimbursement for Bionano’s OGM-based LDTs in hematologic malignancies and complements earlier updates on growing revenue and expanding clinical evidence for OGM. Investors may track how frequently codes 81195 and 81354 are utilized, reimbursement adoption by payers, and the company’s financing activities disclosed in recent SEC filings.

Key Terms

clinical lab fee schedule, clia-certified, laboratory developed tests, optical genome mapping, +4 more
8 terms
clinical lab fee schedule regulatory
"announced today that the clinical lab fee schedule (CLFS) for 2026..."
A clinical lab fee schedule is the list of prices used to bill for medical laboratory tests, often set or influenced by insurers and government payers like Medicare. Think of it as a menu that determines how much a lab can charge or be reimbursed for each test; changes to that menu directly affect a lab’s revenue, profit margins and cash flow, so investors watch fee schedules to gauge future earnings and pricing risk.
clia-certified regulatory
"offering CLIA-certified laboratory developed tests (LDTs)..."
CLIA-certified means a laboratory has passed U.S. federal standards for performing tests on human samples, showing its results are accurate, reliable and timely. For investors this matters because certification is often required to sell clinical test services, bill insurers, win hospital or physician partnerships and avoid regulatory penalties — much like a restaurant passing a health inspection or a car getting a safety sticker before it can be sold.
laboratory developed tests medical
"offering CLIA-certified laboratory developed tests (LDTs) based on..."
Laboratory developed tests are medical diagnostic tests that are designed, built and performed by a single clinical laboratory for use within that same lab rather than sold as a finished product by a manufacturer. For investors, they matter because they represent a faster path to bringing new diagnostics to patients but carry regulatory, reimbursement and scalability risks—think of a chef crafting a custom dish in their kitchen versus a food company mass-producing a packaged item.
optical genome mapping medical
"laboratory developed tests (LDTs) based on optical genome mapping (OGM)..."
Optical genome mapping is a laboratory technique that produces a high-resolution picture of a person’s long DNA strands to find large structural changes such as missing, extra, or rearranged pieces. For investors, it matters because the method can improve diagnosis, speed development of genetic tests and therapies, and influence regulatory approvals and market demand for companies offering more accurate or faster genomic tools — think of it as a wide-angle camera that reveals large-scale defects traditional microscopes might miss.
current procedural terminology regulatory
"for the payment for the Category I Current Procedural Terminology (CPT®) code 81195."
Current Procedural Terminology (CPT) is a standardized set of codes used to describe medical, surgical and diagnostic services for billing and reporting. Think of it as a universal menu of procedure names and prices that hospitals, doctors, insurers and medical device makers use to communicate what was done and get paid. Changes to CPT codes can alter reimbursement, revenue forecasts and competitive positioning across healthcare companies, so investors watch them closely.
hematologic malignancies medical
"use of OGM in cytogenomic genome-wide analysis to detect... related to hematologic malignancies..."
Hematologic malignancies are types of cancers that start in the blood or the organs responsible for blood production, like the bone marrow and lymph nodes. They matter because they can disrupt normal blood functions, leading to issues like weakness, infections, or abnormal growths, and often require specialized treatments.
cytogenomic genome-wide analysis medical
"use of OGM in cytogenomic genome-wide analysis to detect structural..."
A cytogenomic genome-wide analysis is a laboratory test that scans a person’s entire DNA for large-scale and small-scale changes in chromosomes—such as missing, extra, or rearranged stretches of genetic material—by combining chromosome-level and DNA-level methods. Investors should care because these tests drive diagnoses, patient selection for therapies, and regulatory decisions; think of it like a full building inspection that reveals structural defects investors need to value medical products, markets, and reimbursement prospects.
fluorescence in-situ hybridization medical
"alternatives to legacy cytogenetics methods such as karyotyping, fluorescence in-situ hybridization (FISH)..."
Fluorescence in-situ hybridization is a laboratory technique that uses glowing molecular probes to find and highlight specific DNA or RNA sequences inside cells, like placing colored sticky notes on particular sentences in a large book. For investors, it matters because the test can diagnose diseases, identify genetic targets for therapies, and serve as a companion diagnostic that influences clinical decisions, regulatory approval and commercial value for biotech and diagnostics firms.

AI-generated analysis. Not financial advice.

SAN DIEGO, Dec. 03, 2025 (GLOBE NEWSWIRE) -- Bionano Laboratories, a wholly-owned subsidiary of Bionano Genomics, Inc. (Nasdaq: BNGO) offering CLIA-certified laboratory developed tests (LDTs) based on optical genome mapping (OGM), announced today that the clinical lab fee schedule (CLFS) for 2026 posted by Centers for Medicare & Medicaid Services (CMS) indicates an increase of 47%, from $1263.53 to $1853.22, for the payment for the Category I Current Procedural Terminology (CPT®) code 81195. This code applies to use of OGM in cytogenomic genome-wide analysis to detect structural and copy number variations related to hematologic malignancies, or blood cancers.

CMS previously established a payment determination, effective January 1, 2025, for the Category 1 CPT code 81195 at $1263.53 based on a crosswalk to an existing code. A request for reconsideration and crosswalk to a different code with a higher payment rate was made. The clinical diagnostic laboratory test (CDLT) committee that reviews such applications voted unanimously in favor of the proposed crosswalk by a vote of 10-0 with no abstentions. CMS subsequently agreed with the panel and the OGM users who commented as part of the process and re-priced code 81195 to $1853.22, effective January 1, 2026.

CPT codes for OGM are key components for obtaining reimbursement from third party payers for the OGM-based LDTs developed by Bionano Laboratories and used as alternatives to legacy cytogenetics methods such as karyotyping, fluorescence in-situ hybridization (FISH) and microarrays. There are now two such codes, 81195 for use of OGM in hematologic malignancy analysis and 81354 for use of OGM in constitutional genetic disease. Bionano Laboratories has offered OGM-Dx™ HemeOne, OGM-Dx™ Postnatal Whole Genome SV and OGM-Dx™ Prenatal Whole Genome SV, all of which would be expected to be covered by these two codes.

“We believe the increase in the CLFS for the Category 1 CPT code 81195 will make it easier to offer OGM-based LDTs for hematologic malignancies due to the potentially more favorable reimbursement from payers,” said Alka Chaubey, chief medical officer of Bionano. “We believe the newly established payment level, which is substantially higher than the original pricing, is appropriate for the additional data collection, interpretation and reporting needed when using OGM for blood cancers. We also believe that establishing Category I CPT codes can raise the awareness of the utility and support for OGM in the oncology and clinical genetic testing communities, not only in the United States, but around the world as well.”

About Bionano Laboratories:

Lineagen, Inc. d/b/a Bionano Laboratories provides access to genetic answers and support utilizing cutting-edge technologies to advance the way the world sees the genome.  Its clinical diagnostics services offer optical genome mapping (OGM) testing that combines a comprehensive testing portfolio with thoughtful and accessible support options. Bionano Laboratories also offers direct access to OGM for applications across basic, translational and clinical research. For more information, visit www.bionanolaboratories.com

About Bionano 

Bionano is a provider of genome analysis solutions that can enable researchers and clinicians to reveal answers to challenging questions in biology and medicine. The Company’s mission is to transform the way the world sees the genome through optical genome mapping (OGM) solutions, diagnostic services and software. The Company offers OGM solutions for applications across basic, translational and clinical research.  The Company also offers an industry-leading, platform-agnostic genome analysis software solution, and nucleic acid extraction and purification solutions using proprietary isotachophoresis (ITP) technology. Through its Lineagen, Inc. d/b/a Bionano Laboratories business, the Company also offers OGM-based diagnostic testing services.

For more information, visit www.bionano.com or www.bionanolaboratories.com

Unless specifically noted otherwise, Bionano’s products are for research use only and not for use in diagnostic procedures.

Forward-Looking Statements of Bionano Genomics

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995.  All statements other than statements of historical facts contained in this press release, including statements regarding our future results of operations or financial condition, business strategy and plans, and objectives of management for future operations, are forward-looking statements. Words such as “anticipate,” “believe,” “can,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “target,” “will,” or “would” and similar expressions (as well as other words or expressions referencing future events, conditions or circumstances) convey uncertainty of future events or outcomes and are intended to identify these forward-looking statements. Forward-looking statements include statements regarding our intentions, beliefs, projections, outlook, analyses or current expectations concerning, among other things; the ability and utility of the Category I CPT code to drive use and adoption of our OGM-based tests; the ability of the OGM-Dx tests to obtain coverage and reimbursement; whether the Category I CPT code will ultimately be important for clinical OGM testing; the ability of OGM to outperform legacy cytogenomic methods; our expectations regarding product uptake, revenue, flowcell usage by customers we consider to be routine users of OGM, market development and OGM adoption, including as evidenced through publications highlighting the utility and applications of OGM, our commercial prospects and future financial and operating results; continued research, presentations and publications involving OGM, its utility compared to traditional cytogenetics and our technologies; and our ability to drive adoption of OGM and our technology solutions and any other statements that are not of historical fact. Each of these forward-looking statements involves risks and uncertainties. Accordingly, investors and prospective investors are cautioned not to place undue reliance on these forward-looking statements as they involve inherent risk and uncertainty (both general and specific) and should note that they are provided as a general guide only and should not be relied on as an indication or guarantee of future performance. Actual results or developments may differ materially from those projected or implied in these forward-looking statements. Factors that may cause such a difference include the risks and uncertainties associated with: the failure of the Category I CPT code to drive use and adoption of our OGM-based tests; the failure of our tests to obtain coverage and reimbursement; the failure of the Category I CPT code to prove to be important for clinical OGM testing; the failure of OGM to outperform legacy cytogenomic methods; the timing and amount of revenue we are able to recognize in a given fiscal period; our ability to obtain sufficient financing to fund our strategic plans and commercialization efforts and our ability to continue as a “going concern,” which requires us to manage costs and obtain significant additional financing to fund our strategic plans and commercialization efforts; the risk that if we fail to obtain additional financing we may seek relief under applicable insolvency laws; the impact of adverse geopolitical and macroeconomic events, such as the ongoing conflicts between Ukraine and Russia and Israel and Gaza and uncertain market conditions, including inflation, tariffs, and supply chain disruptions, on our business and the global economy; general market conditions; changes in the competitive landscape and the introduction of competitive technologies or improvements to existing technologies; changes in our strategic and commercial plans; the ability of medical and research institutions to obtain funding to support adoption or continued use of our technologies; study results that differ or contradict the results mentioned in this press release; the risk that we are not able to complete a strategic transaction that would increase stakeholder value; and the risks and uncertainties associated with our business and financial condition in general, including the risks and uncertainties including those described in our filings with the Securities and Exchange Commission (“SEC”), including, without limitation, our Annual Report on Form 10-K for the year ended December 31, 2024, our Quarterly Reports on Form 10-Q  and in other filings subsequently made by us with the SEC. All forward-looking statements contained in this press release speak only as of the date on which they were made and are based on management’s assumptions and estimates as of such date. We do not undertake any obligation to publicly update any forward-looking statements, whether as a result of the receipt of new information, the occurrence of future events or otherwise, except as may be required by law.

CONTACTS

Company Contact:
Erik Holmlin, CEO
Bionano Genomics, Inc.
+1 (858) 888-7610
eholmlin@bionano.com

Investor Relations:
Kelly Gura
Gilmartin Group
+1 (858) 888-7625
IR@bionano.com


FAQ

What change did CMS make to CPT code 81195 for BNGO on December 3, 2025?

CMS re-priced Category I CPT code 81195 from $1,263.53 to $1,853.22, a 47% increase, effective January 1, 2026.

How did the CDLT committee vote on the crosswalk supporting CPT 81195 for BNGO's OGM use?

The clinical diagnostic laboratory test committee voted 10-0 in favor of the proposed crosswalk with no abstentions.

Which tests from Bionano Laboratories are expected to be covered by the CPT code changes?

Bionano Laboratories expects OGM-based LDTs including OGM-Dx HemeOne, OGM-Dx Postnatal Whole Genome SV, and OGM-Dx Prenatal Whole Genome SV to be covered by the relevant CPT codes.

When does the new payment level for CPT 81195 take effect for Medicare?

The new payment level for CPT 81195 is effective January 1, 2026.

What does the CPT 81195 re-pricing mean for BNGO reimbursement prospects?

The company says the higher CLFS rate should make it easier to offer OGM-based LDTs due to potentially more favorable reimbursement from payers.

Are there other CPT codes for OGM besides 81195 relevant to BNGO?

Yes; CPT 81354 covers OGM use in constitutional genetic disease, while 81195 covers hematologic malignancy analysis.
Bionano Genomics Inc

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Medical Instruments & Supplies
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SAN DIEGO