Life Science Outsourcing

Fluid Management Device Expertise

Accelerate fluid management device production with LSO’s assembly, packaging, and sterilization services—scalable, compliant, and fast to market.

Fluid Management Device Expertise
FDA-Registered Manufacturing FacilityISO 13485 Certified Quality System12 Cleanrooms Class 5–8125,000+ Sq Ft Regulated Manufacturing3 Facilities CA | NH | Costa Rica
Technician Assembling Fluid Management Device in Cleanroom – LSO

End-to-End Assembly, Kitting, Packaging, and Sterilization Services

Fluid Management Device Expertise

Fluid management devices play a critical role in surgical, diagnostic, and therapeutic applications, requiring precision manufacturing, rigorous sterilization, and full regulatory compliance. OEMs in this sector must navigate complex FDA and ISO requirements while ensuring the reliability and sterility of their devices.

LSO partners with leading and emerging medical device manufacturers to provide scalable, compliant, and cost-effective solutions for fluid management device assembly, packaging, and sterilization. Our integrated services help streamline production and ensure a faster path to market—without sacrificing quality.

Fluid Management Device Capabilities

Life Science Outsourcing provides specialized expertise in the manufacturing, packaging, and sterilization of fluid management devices.

Life Science Outsourcing, Inc.

Cleaning & Decontamination

We ensure fluid management devices are free from contaminants and biohazards, meeting stringent sterility and safety standards.

Cleanroom Assembly & Kitting

From precision tubing assemblies to complete fluid management kits, LSO delivers turnkey cleanroom manufacturing and kitting solutions.

Technician Assembling Fluid Management Device in Cleanroom – LSO

Labeling

Our in-house labeling capabilities ensure full compliance with FDA, ISO, and UDI (Unique Device Identification) regulations, supporting both single-use and reusable fluid management devices.

Sterilization

LSO offers comprehensive contract sterilization services with validation support to ensure regulatory compliance and patient safety.

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Product Portfolio

  • IV sets and infusion systems
  • Catheters (vascular, urinary, and drainage)
  • Blood collection and transfusion sets
  • Suction and aspiration devices
  • Dialysis tubing and connectors
  • Irrigation and fluid warming systems
  • Negative pressure wound therapy (NPWT) components

Why LSO?

Specialized Expertise for Fluid Management Device OEMs

Fluid management devices require precision, sterility, and compliance to ensure patient safety and product performance. LSO’s integrated solutions help manufacturers streamline production while meeting strict regulatory standards.

  • Faster Time-to-Market
    Accelerate FDA and ISO approvals with seamless cleanroom assembly, packaging, and sterilization services.
  • Comprehensive Compliance Support
    Navigate complex regulatory requirements with our in-depth expertise in FDA, ISO 13485, and biocompatibility standards.
  • Cost-Effective, Scalable Solutions
    Reduce costs with fully integrated in-house services, supporting both clinical trials and commercial production.
  • End-to-End Manufacturing & Sterilization Expertise
    From device assembly and kitting to validated sterilization and regulatory documentation, we provide a one-stop solution for fluid management device manufacturers.

FDA-Registered

Manufacturing Facility

ISO 13485

Certified Quality System

12 Cleanrooms

Class 5–8

125,000+ Sq Ft

Regulated Manufacturing

3 Facilities

CA | NH | Costa Rica