MPT Quick Quote Thank You
FDA-Registered Manufacturing FacilityISO 13485 Certified Quality System12 Cleanrooms Class 5–8125,000+ Sq Ft Regulated Manufacturing3 Facilities CA | NH | Costa Rica
An LSO specialist will contact you within 1 business day (2 days at most) to discuss your project and next steps.
If your request is urgent, please call us at 714-672-1090.
Why medical device manufacturers choose LSO
• FDA-registered, ISO 13485-certified
• 25+ years supporting Class I, II, and III devices
• In-house assembly, packaging, sterilization, and testing
• Fast project onboarding with regulatory guidance
What to expect next
• We’ll review your project details
• A specialist will reach out by phone or email
• We’ll outline timelines, documentation, and next steps
Explore LSO capabilities
Resources our clients find helpful:
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