Life Science Outsourcing

Medical Device Manufacturing That Scales With Your Success

FDA-registered contract manufacturer supporting 820+ successful device launches with ISO 13485 certified processes across assembly, packaging, sterilization, and fulfillment.

Medical Device Manufacturing That Scales With Your Success
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
ISO 17025
Accredited Packaging Lab

Proven Results Across 25+ Years

820+

Startup Launches

$4B+

Client Acquisition Value

125K+

Sq Ft Manufacturing

12

FDA Cleanrooms

End-to-End Medical Device Contract Manufacturing

Life Science Outsourcing provides comprehensive contract manufacturing services for medical device companies, from early-stage startups to established enterprises. Our FDA-registered facilities in California, New Hampshire, and Costa Rica deliver scalable solutions that grow with your business.

With ISO 13485 certification and expertise across assembly, packaging, sterilization, and distribution, we eliminate the complexity of bringing medical devices to market while ensuring regulatory compliance at every step.

Complete Manufacturing Capabilities Under One Roof

From prototype to commercial scale, we handle every aspect of medical device production

Assembly & Kitting

Precision assembly in Class 5-8 cleanrooms with documented procedures and full traceability

Packaging & Validation

ISO 11607 sterile barrier packaging with accelerated aging and transit validation

Sterilization Services

EtO, gamma, and steam sterilization with ISO 11135/11137/17665 validation protocols

Quality & Compliance

FDA 21 CFR Part 820 (QMSR) compliance with lot genealogy and complete documentation

Global Distribution

Fulfillment and logistics services with temperature-controlled storage capabilities

Rapid Scale-Up

Flexible capacity across three facilities to meet demand fluctuations and growth

Our Manufacturing Process

1

Project Assessment

We evaluate your device requirements, regulatory needs, and production timeline to develop a comprehensive manufacturing plan

2

Process Development

Our engineering team designs and validates manufacturing processes, creates work instructions, and establishes quality controls

3

Pilot Production

Small-scale production runs verify processes, identify optimization opportunities, and ensure consistent quality output

4

Scale-Up & Launch

Full commercial production with real-time monitoring, lot genealogy tracking, and continuous improvement protocols

Trusted by Medical Device Leaders

We have been extremely impressed with LSO’s responsiveness, integrity, technical knowledge, attention to detail, passion for schedule and value. They surpass many of the larger more well known labs in all of these categories. LSO is our new go-to vendor for laboratory services!

BD

Bob, Director of Research

Orthopedic device company

From day one LSO has exceeded our expectations. All the divisions we have worked with have been professional, knowledgeable, easily accessible and quickly responsive. The attention to detail and communication has been terrific. We are very happy we found LSO. They have met all our needs and then some!

JD

Jeff, Director of Operations

Orthopedic device company

...the team at LSO have been great to work with. Their decades of experience in packaging, sterilization, and validation, helped us accelerate the release of our medical device in record time.

GC

Goutam, CEO

Specialty kits manufacturer

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

ISO 17025

Accredited Packaging Lab

Ready to Scale Your Medical Device Manufacturing?

Get a custom manufacturing plan with timeline and cost estimates for your device.

Or call us directly: (714) 672-1090