Metal Springs & Stamped Parts for Inhalers

Precision springs and metal components for respiratory drug delivery devices

How RPK Medical supports inhaler manufacturers, from prototype to full-scale production

10/05/2026

Inhaler manufacturers face a hard constraint: the metal parts inside a device must meet micron-level tolerances, pass biocompatibility requirements, and provide full batch traceability — every time, at scale. RPK Medical manufactures precision springs, stamped parts, and bent metal components specifically for MDI, DPI, and SMI respiratory devices. We work with you from the first design review through serial production.

MDI, DPI, and SMI: What Makes Each Device Different

Each inhaler platform puts different demands on its metal components.

MDI
Metered-Dose Inhaler

A pressurized canister releases a fixed drug dose through a metering valve. The valve spring controls that release. New low-GWP propellants — HFO blends replacing HFA 134a — change internal pressure profiles, which means spring force specs need to be re-engineered, not simply carried over.

 
DPI
Dry Powder Inhaler

No propellant. The patient's breath drives drug delivery. Springs and stamped contact parts manage airflow resistance, dose consistency, and actuator feedback. Tolerances are tight because there's no propellant pressure to compensate for variation.

 
SMI
Soft Mist Inhaler

A calibrated spring drives a mechanical pump that atomizes the liquid formulation. Spring force directly determines droplet size — and droplet size determines where the drug deposits in the lung. Get the spring wrong and the therapy fails.

 

New Challenges Facing Inhaler Component Buyers

The regulatory and commercial environment is changing fast.

New propellantsHFO and CO₂-based systems operate at different pressures than legacy HFA propellants. Springs must be re-validated, material selection and load specs both shift.
Dosage accuracyFDA and EMA are tightening requirements on dose uniformity. That pressure flows directly to component suppliers: tighter CPK requirements, mandatory SPC monitoring, lot-level dimensional records.
SustainabilityMedical device OEMs are tracking material footprint. Stamping scrap rates, alloy recyclability, and packaging all fall under supplier review.
IndustrializationMoving from a validated prototype to 20 million parts per year without dimensional drift is a manufacturing problem, not just a quality one. The process has to be built for scale from the start.

Critical Metal Components for Respiratory Devices

RPK Medical produces the metal parts that sit at the functional core of inhalers.

ComponentApplicationSpecifications
Valve springsMDI metering valve dose release controlCompression & torsion. Tolerances ±0.02 mm wire diameter, ±0.5% spring rate. Materials: SS 302/304, Elgiloy, MP35N
Stamped parts & contact partsActuators, dose counters, locking mechanismsProgressive die production with in-line vision inspection. Full dimensional traceability per batch
Bent metal componentsClips, retention brackets, guide featuresFormed to customer drawings. Suitable for cleanroom-compatible alloys and surface finishes
All parts are deburred, cleaned, and inspection-documented before shipment — ready for direct integration into device assembly.

Why RPK Medical

01

Cleanroom production

Metal forming and finishing take place in controlled environments designed for medical component manufacturing. Particulate control runs from stamping through final packaging.

02

Full traceability

Every batch ships with material certifications, dimensional inspection reports, and process records. Documentation aligns with ISO 13485 and FDA 21 CFR Part 820.

03

Design for manufacturability

RPK engineers engage early. We review drawings before tooling is cut, flag tolerance stack-up risks, and propose geometry changes that reduce cost without affecting function.

04

Volume flexibility

We run prototype quantities and 50M+ parts per year on the same quality system. Scaling up does not mean starting over.

05

Cross-sector process depth

RPK serves automotive, e-mobility, and industrial markets alongside medical. Process disciplines from high-volume automotive stamping transfer directly into medical production.

From design to production: how we work with you

1 | Feasibility review

Share your drawing or concept. We assess manufacturability, flag risks, and return written feedback. No commitment required.

2 | Prototype and validation

We produce the first articles, support PPAP documentation, and provide dimensional and functional data for your validation package.

3 | Serial production

Parts transfer to high-speed stamping lines with full SPC monitoring active. You get the same contact, the same quality records, and the same dimensional targets at volume.

One team handles all three phases. There is no handoff between an engineering group and a production group; the people who designed the process run it.

Frequently Asked Questions

What spring materials are compatible with new low-GWP propellants?

Stainless 302 and 304 perform well in most HFO environments. For aggressive formulations or elevated humidity, Elgiloy and MP35N offer better corrosion resistance and fatigue life. RPK will recommend the right alloy based on your specific propellant and pressure profile.

Do you produce parts under ISO 13485?

Yes. RPK Medical operates under a quality management system aligned with ISO 13485 and FDA 21 CFR Part 820. Full documentation is available on request.

Can you handle both prototype and mass production?

Yes, from single prototypes through tens of millions of parts per year, with the same traceability at every stage.

Let’s talk and turn concerns into certainties. Tell us!

Get in touch with our engineering and sales teams, we’ll listen to you carefully and find the best solution together.

Contact us now