Medical Device Component Manufacturing/San Clemente, CA

The quality system behind every part we mold.

IRP Medical manufactures custom silicone and rubber components for medical devices under an ISO 13485:2016 quality management system, FDA registered, with ISO Class 8 cleanroom environment molding, in San Clemente, California. This page is the reference for your supplier qualification: certifications, cleanroom, and how parts are inspected, validated, documented, and traced.

ISO 13485:2016 · BSI FM 590598/ FDA-Registered/ ISO Class 8 Cleanroom Environment Molding/ Made in the USA/ 24/7 Operations
Certifications

ISO 13485:2016 certified.
FDA registered.

The two claims a sourcing engineer checks first, stated plainly, with the certificate available for download.

Quality Management System

ISO 13485:2016

IRP Medical is certified to ISO 13485:2016, the quality management standard for medical devices. The certificate scope reads “Custom Critical-To-Function Engineered Components”: the work itself, stated on the certificate.

Certificate scope“Custom Critical-To-Function Engineered Components”
U.S. Food and Drug Administration

FDA Registered

IRP Medical's manufacturing facility in San Clemente, California is registered with the U.S. Food and Drug Administration. Registration details are available to customers as part of supplier qualification.

Registered establishment1035 Calle Amanecer, San Clemente, CA 92673
Details in supplier qualification Request registration details
Download ISO 13485 Certificate (PDF)
Cleanroom

ISO Class 8 cleanroom environment molding.

Gowned operator at an automated production cell in the IRP Medical ISO Class 8 cleanroom environment
ISO Class 8

Contamination control isn't a finishing step. It's the environment the part is made in.

Molding at IRP Medical runs in one ISO Class 8 cleanroom environment, under the ISO 13485:2016 quality management system.

Molding processes
Liquid injection moldingGum moldingCompression rubber moldingTransfer moldingOvermolding / insert molding
Quality System

Inspected, validated,
documented, traceable.

The four things your quality team will verify, and how each one works here. Certification is the given. This is what runs underneath it, lot after lot.

Inspection

Automated non-contact vision metrology, custom inspection solutions engineered per program, and functional testing, inflation and leak, where the part demands it.

Validation

IQ/OQ/PQ process validation, supported by FAI, MSA, and DOE.

Documentation

The quality management system is integrated with the ERP, and records are built as the work happens: audit-ready any day, not audit day.

Traceability

Complete material and product traceability, lot by lot, from raw material receipt to shipped component.

FAQ

Quality questions, answered plainly.

Is IRP Medical ISO 13485 certified?
Yes. IRP Medical is certified to ISO 13485:2016, the quality management standard for medical devices. The certificate scope reads “Custom Critical-To-Function Engineered Components”: the work itself, stated on the certificate. The certificate is available for download on this page.
Is IRP Medical FDA registered?
Yes. IRP Medical's manufacturing facility in San Clemente, California is registered with the U.S. Food and Drug Administration. Registration details are available to customers as part of supplier qualification.
What class is IRP's cleanroom?
ISO Class 8. Molding at IRP Medical runs in an ISO Class 8 cleanroom environment.
Is IRP ISO 9001 certified?
No. ISO 13485 is the quality management standard specific to medical devices, and it supersedes ISO 9001 for this work. A supplier certified to ISO 13485:2016 is held to the more demanding, medical-device-specific standard; a separate ISO 9001 certificate would add nothing to it.
Can I get a copy of IRP's certifications?
Yes. The ISO 13485:2016 certificate is available for download on this page, and supporting quality documentation is available on request as part of supplier qualification.
Next Step

Put us through your
supplier qualification.

New program or supplier transfer,
it starts with the print.

Starting a new program?

From clinical builds to commercial scale, engage our engineers at the print.

Start Your Program

Transferring a program or mold?

Revalidation is a given. We plan it around your inventory bank, so your line keeps running while we qualify.

Transfer Your Program
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