
BioAssemblyBot® 500 is a high-throughput, six-axis biofabrication system designed for scalable, reproducible tissue engineering. Fully integrated within a Class II, Type-A biosafety cabinet, BAB 500 delivers unmatched environmental control, sterility, and precision, enabling life scientists to build, nurture, and translate complex 3D biological systems into real-world therapeutic solutions.
This is advanced biofabrication at clinical scale.
Building 3D biology for humans.


BioAssemblyBot® 500 Key Specifications
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Six-axis robotic biofabrication system for complex, high-throughput workflows
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Integrated Class II, Type-A biosafety cabinet for sterile, controlled operation
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Supports up to 10 BioAssemblyBot Hands in a single automated run
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Temperature-controlled biofabrication (hot, cold, and ambient workflows)
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Pneumatic and mechanical dispensing for diverse biomaterials
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Machine vision with adaptive tip detection for precision and consistency
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HEPA filtration with 99.97% efficiency at 0.3 µm
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Touchscreen-controlled interface with integrated workflow management
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Powered lift base for ergonomic and system-level access
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Designed for organoids, NAMs, drug discovery, and translational research
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Built for scalable, reproducible, clinically relevant tissue production

BioAssemblyBot500 Features


BioAssemblyBot 500 is the only six-axis biofabrication device with an integrated Class II, Type-A biosafety cabinet. BAB500 can be easily taught to translate your biology recipe into clinical solutions.
BioAssemblyBot 500 Key Features & Specifications:
UL cGMP Certified
HEPA Filtration System
Class II, Type-A Biosafety Cabinet
6-Axis Robotic Arm
Touch Screen Control Panel
Temperature Controlled Print Stage
Adaptive Tip Detection
Use up to 10 BioAssemblyBot Hands

Required electrical cabinet not shown.


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The Advanced Solutions Louisville, KY facility has been audited by UL Registrar LLC and meets GMP requirements listed in RCP, NBCP, or Pharmaceutical Certification Schemes which is uniquely accredited by the American National Standard Institute (ANSI) developed in accordance with applicable sections of the FDA’s code of federal regulations.









