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FDA registered · ISO 13485 QMS · cGMP

Medical Device Machining & Contract Manufacturing in Florida.

Contract manufacturing for medical device OEMs who need a supplier that already speaks their quality language — ISO 13485, cGMP, validated processes, and complete traceability.

Why teams choose MTE

Built for medical device.

01

Built for audits

FDA registered since 2004, with an ISO 13485-conforming quality system, controlled documents, and records ready for your supplier audit.

02

Validated processes

IQ/OQ/PQ support so your process is locked before full-rate production.

03

Biocompatible materials

Titanium, 316L, PEEK, and Nitinol with full material certification.

What we make

Typical parts.

Don't see yours? Send the print — if it's tight-tolerance and machinable, we probably make something like it.

  • Surgical instruments
  • Orthopedic implants & screws
  • Endoscopic components
  • Diagnostic housings
  • Robotic surgery parts
Capabilities

The processes behind it.

Other industries
Request a quote

Send us your print.
Get a real answer.

Our engineers review every drawing for manufacturability and return a detailed quote — typically within 48 hours. Confidential, with an NDA on request.

  • NDA on request
  • DFM feedback included
  • Direct line to an engineer