News Archives - Pathway | New Product Development

Medical device team reviewing a catheter design and engineering documentation for FDA clearance.

August 26, 2026

How to Prepare Your Medical Device for FDA Clearance

August 19, 2026

Medical Device Packaging Services

August 11, 2026

Medical Device Manufacturing Transfer Checklist

August 5, 2026

When Do You Need ISO 13485 for Medical Device Manufacturing?

July 28, 2026

Why Low-Volume Medical Device Manufacturing Matters Before Scale

July 24, 2026

Choosing a Medical Device Contract Manufacturer in San Diego

July 14, 2026

What Is Design for Manufacturability in Medical Devices?

June 17, 2026

What Is a 510(k) Submission and How It Works

June 9, 2026

Digital Health and Connected Devices

ISO Class 7 cleanroom at Pathway Medtech facility

March 20, 2026

Pathway Medtech Announces Completion and Certification of Fourth ISO Class 7 Cleanroom