In industrial equipment, even small part failures can shut down production.
Gromax delivers rugged, precision-stamped components built to tight tolerances and quality standards—helping OEMs and Tier 1/2 suppliers build durable, reliable equipment with confidence.
✅ Helps prevent late-stage redesigns or sterilization incompatibilities.
We collaborate with your engineers to optimize stamped components for biocompatibility, sterilization compatibility, and dimensional accuracy—reviewing material certifications, surface finish requirements, and manufacturability.
✅ Speeds up regulatory submission timelines and design verification.
Accelerate device validation with production-intent prototypes for housings, frames, contacts, or shields—enabling design verification and functional testing before scaling.
✅ Delivers tooling that meets medical device tolerances and traceability.
Our in-house die shop builds progressive dies capable of stamping medical-grade materials (316L stainless steel, titanium, MP35N, nitinol) with precision coining, embossing, and formed features.
✅ Ensures dimensional integrity and cleanliness for assembly into medical systems.
We achieve tolerances down to ±0.0015” with clean shearing and burr control to support mechanical fit, clean assembly interfaces, and surface finish readiness for sterilization.
✅ Reduces multi-supplier coordination and ensures regulatory-compliant finishes.
We coordinate passivation, polishing, electropolishing, or plating (tin, silver, gold to ASTM/FDA specs)—delivering clean, assembly-ready components for medical devices.
✅ Supports source inspection, AS9100 flows, and readiness for production qualification audits.
Every component ships with full documentation (PPAP, FAIR, CMM, material certs, lot traceability), supporting ISO 13485, FDA, and customer-specific validation requirements.
We achieve tolerances down to ±0.0015” to ensure critical fit and function in life-saving devices.
We deliver passivation, electropolishing, and plating processes compliant with ASTM/FDA standards.
We minimize burr height to protect sensitive assemblies and reduce contamination risks
Every lot is traceable to material certs and process records to support FDA, ISO 13485, and supplier audits.
We deliver comprehensive documentation for design history files, supplier validation, and regulatory submissions.
Our engineers collaborate to optimize design for manufacturability and sterilization (gamma, EO, autoclave
We use precision die design and in-die deburring to control burrs at the stamping stage, delivering components suitable for medical assembly and sterilization.
We source DFARS-compliant materials with full traceability and material certs for implantable and Class III devices.
We deliver PPAP, FAIR, CMM, and material certs with each lot—ready for your design history file and regulatory submission.
We deliver integrated passivation, electropolishing, and plating services, reducing vendor coordination and ensuring process control.
We maintain critical dimensions with progressive die process control, validated by in-process and final CMM inspection.
Upload your drawing or RFQ to request a quote for precision-stamped, compliance-ready medical components built to your production needs.