Medora™ is Biomedisca's flagship investigational point-of-care test under development. It is designed to use a small fingerstick blood sample to provide an inflammatory-risk screening signal during a dental visit, alongside periodontal findings and medical history.
Targeting a binary screening signal in approximately 15 minutes without a separate reader. Finished-product performance requires verification.
Medora is under development, has not been cleared or approved by the U.S. FDA, and is not currently available for clinical use or sale.
Periodontal inflammation is usually evaluated and treated within the dental setting, but the inflammatory picture may extend beyond the mouth. Medora is designed to bring rapid inflammatory screening into the same dental visit, helping dental professionals recognize when additional health awareness and medical follow-up may be appropriate.
The patient presents with signs of periodontal inflammation during a routine dental visit.
A rapid fingerstick-based Medora test provides inflammatory biomarker information during the same visit.
The result supports broader health awareness and can help determine when appropriate medical follow-up should be considered.
“The goal is not to diagnose systemic disease in the dental office—it is to identify an inflammatory signal that should not be overlooked.”
Medora is an investigational device under development and has not been cleared by the FDA.
Rapid screening integrated into the existing dental workflow.
Designed as an easy-to-use binary rapid test without complex instrumentation.
Helps move care from reacting to disease toward earlier health awareness.
Creates a practical bridge between oral-health findings and appropriate medical follow-up.
Periodontal inflammation and systemic inflammatory burden may coexist, but dental professionals currently lack a practical same-visit tool for evaluating this relationship. Medora is being developed to help close that clinical information gap.
A small whole-blood sample is collected from the patient during the visit.
The blood sample is prepared with the supplied buffer for testing.
The prepared sample is added directly to the Medora test cassette.
The integrated test architecture separates plasma and moves the sample across the detection membrane.
Two complementary inflammatory signals are evaluated simultaneously within a single test.
Visible test lines are intended to provide a binary screening signal in approximately 15 minutes without a separate reader. These are development targets.

Concept illustration of the proposed test architecture. Collection, preparation, test-line interpretation, timing, and reader-free use require verification in the finished product.
Medora's intended output is a binary screening signal. The illustrations below describe the proposed interpretation, which requires validation; they are not patient results or disease-risk grades.
The intended positive output would indicate the target inflammatory signal. It would not identify the source of inflammation or diagnose systemic disease. Any future follow-up would depend on the complete clinical assessment.
The intended negative output would indicate that the target screening signal was not detected. It would not exclude cardiovascular disease, systemic inflammation, or another medical condition.
Warning: Medora is a screening tool under development. It is not intended to independently diagnose, treat, prevent, or rule out any disease.
Routine dental and periodontal assessment.
Identify a patient who may benefit from additional inflammatory-risk screening.
If validated and authorized, perform Medora testing during the same visit.
Review the binary result alongside medical and dental history.
Provide education and consider appropriate follow-up.
Repeat screening when clinically appropriate after the product is authorized for use.
This is an intended future workflow, subject to validation and applicable authorization. Medora is not currently available for clinical use.
Medora's intended benefits across dental and medical care require product-specific evaluation.
Published oral–systemic research provides scientific background. Medora’s performance and clinical usefulness require product-specific validation.
Peer-reviewed research describing associations among periodontal inflammation, systemic inflammatory burden, and cardiovascular health.
Background scientific evidenceMedora’s investigational screening methodology is under development. Its performance must be established through product-specific validation.
Development programProduct-specific validation is needed to establish analytical performance, fingerstick-to-reference agreement, reliability in dental-office workflows, and clinical usefulness.
Validation requirementsBackground scientific evidence — these publications describe the oral–systemic research landscape; they are not direct validation of Medora.
Bridging oral and systemic health: exploring pathogenesis, biomarkers, and diagnostic innovations in periodontal disease
Published in Infection — Springer
Periodontal biomarkers in cardiovascular disease: mechanisms, diagnostics, and clinical implications
Published in Infection — Springer
Association between periodontal pathogens and systemic disease
Published in Biomedical Journal
These publications provide scientific background and are not product validation. Explore the Science & Development page for development requirements, or browse Publications.
FDA review has not begun.
Prototype development
Analytical verification
Prospective clinical validation
Regulatory submission
Point-of-care authorization
Commercial introduction
Regulatory submission, point-of-care authorization, and commercial introduction depend on prospective study outcomes and applicable regulatory review.
We welcome clinical research collaborations, strategic partnerships, and investor inquiries.
Explore the product details, scientific context, and next steps that matter to you.