Lab-quality results within minutes, at the point-of-care!
Abionic is a pioneering Swiss MedTech company focused on transforming diagnostics through nanofluidics. Recognized as "Swiss MedTech of the Year" in 2023 and the recipient of multiple industry accolades, Abionic is dedicated to delivering rapid, lab-quality diagnostic solutions at the point of care.
Abionic's flagship product, the abioSCOPE®, is a near-patient rapid diagnostic platform that provides lab-quality results from a single drop of blood within minutes. This innovative technology delivers valuable clinical insights and actionable information, empowering healthcare professionals to make informed decisions swiftly and efficiently. The primary address of Abionic is Biopôle, Rte de la Corniche 3, Sect. Esplanade SE-A, Epalinges, Canton de Vaud 1066, CH.
Abionic is committed to advancing healthcare through cutting-edge diagnostic solutions. We invite the management team at Abionic to create a customized and exclusive company showcase and product listing on our platform, further highlighting their contributions to the medical technology field.
Compare Abionic with 2 companies in Medical-Equipment-Manufacturing
| Comparison Field |
Ab
AbionicMain Company |
GenMark DiagnosticsView Profile |
IMed Consultancy LtdView Profile |
|---|---|---|---|
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Founded Year
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— | 0 | 2012 |
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Company Size
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— | 501-1,000 | 11-50 |
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City
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Epalinges, Canton de Vaud | Carlsbad, CA | Bloxham, England |
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Country
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United States | ||
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Skills & Keywords
Comparing with main company
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12 Total Skills
Medical Technology
Diagnostics
Nanofluidics
Point-of-Care Diagnostics
Rapid Diagnostics
Medical Devices
Healthcare Solutions
IVD diagnostics
Point-of-Care testing
Biomedical Optics
IVD
In Vitro Diagnostics
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13 Total
1 Common
12 Unique
Match
8%
Common Skills:
Medical Devices
Unique Skills:
Data Management
Electrochemical Detection
eSensor
Infectious Diseases
Long Term Partner
Multiplex Molecular Diagnostics
+6
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21 Total
1 Common
20 Unique
Match
8%
Common Skills:
Medical Devices
Unique Skills:
21 CFR Part 820
510k
Auditing
CE Marking
Clinical Evaluations
FDA
+14
|
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