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Six capabilities, one quality system
Everything a device needs between design freeze and shipment, in one building and under one set of procedures.
Precision Machining
Swiss CNC Machining
Implants, bone screws, and instrument components in titanium, cobalt chrome, PEEK, and 300 and 400 series stainless.
- Swiss-type lathes to 32 mm bar
- Tolerances to +/- 0.0002 in
- Thread whirling for bone screws
- Passivation and electropolish
Micro Molding
Medical Injection Molding
Micro and precision molding in medical-grade resins, with scientific molding and cavity pressure monitoring on every press.
- Presses from 15 to 220 tons
- Shot weights under 0.1 g
- Insert and overmolding
- PEEK, PC, COC, and LSR
Cleanroom
Cleanroom Assembly
Finished device and subassembly work in an ISO Class 7 cleanroom, including bonding, tipping, and functional testing.
- 12,000 sq ft ISO Class 7
- UV and solvent bonding
- Catheter tipping and forming
- Leak, flow, and pull testing
Laser Processing
Laser Marking and Welding
UDI laser marking that survives passivation and repeated sterilization, and fine laser welding for instruments and housings.
- UDI and GS1 DataMatrix marking
- Fiber and ultrafast lasers
- Hermetic and spot welding
- Mark verification to ISO 29158
Packaging
Sterile Packaging
Pouch and tray sealing with validated parameters, labeling, and managed sterilization through qualified EO and gamma partners.
- Validated pouch and tray sealers
- Seal strength and dye testing
- Managed EO and gamma sterilization
- Label and IFU control
Engineering
DFM and New Product Introduction
Design for manufacturability reviews, prototype builds, and process development that turns your design into a repeatable, documented process.
- DFM review within five days
- Prototype and pilot builds
- pFMEA and control plans
- IQ, OQ, and PQ protocols
From Drawing to Production.
How a new program moves through Lindqvist
DFM Review
Written manufacturability findings on your design within five business days.
Prototype
Parts built on production-intent equipment so early data carries forward.
Process Development
pFMEA, control plans, and fixtures built around your critical features.
Validation
IQ, OQ, and PQ executed and reported under your change control.
Production
Scheduled production with device history records shipped with every lot.
Starting a new program?
Bring Us In Before the Design Freezes. It Costs Less for Everyone.
A tolerance that adds a secondary operation or a material that needs a new supplier is easy to change on paper and expensive to change after verification testing.
How our NPI process worksGet a free design for manufacturability review on your next device.
- Written findings within five business days
- Cost drivers ranked by impact
- No obligation to build with us
Talk to a Program Manager(763) 555-0148