In medical devices, dimensional stability and material integrity aren’t optional—they’re regulatory requirements. If forming or plating distorts thin parts, or tolerance drift causes leaks, seizure, or bad readings, compliance is at risk and launches stall.
Gromax designs, builds, stamps, and inspects under one roof, keeping every step traceable and verified. Our DFM, tooling, stamping, and gaging teams work together so parts stay stable through forming, plating, sterilization, and assembly—precision you can validate and prove to any auditor.
PPAP/FAI, lot-level certs, GR&R ≤10% on CTQs, and controlled special processes tied to part numbers.
Materials/finishes proven for EtO, gamma, and autoclave (passivation, electropolish, Ni/Pd-Ni/Au, Sn) without drift or discoloration.
±0.0015″ features, tight true-position, and ≤0.10 mm coplanarity; coined flats and downset control for shields and leadframes.
BeCu/bronze springs with tuned normal force, selective Au/Pd-Ni on wipe, and burr direction managed away from mating.
Carriers engineered for insert/overmold transfer, pick-and-place features, in-reel orientation, and clean break tabs to cut scrap.
Glove handling, low-lint packs, RoHS-compliant chemistries, surface roughness control, and plating microsections for release.
Yes. We stamp stainless steel, nickel silver, and beryllium copper under validated process controls.
Yes. Every lot includes FAIR/PPAP, control plan, inspection data, and full material traceability.
While not certified, our quality system aligns with ISO 13485 principles and supports OEM documentation standards.
Yes — we design carriers and datums that align perfectly with molding partners for clean insert performance.
Upload your drawing or RFQ to request a quote for precision-stamped, compliance-ready medical components built to your production needs.