Manufacturer of Sterile Procedure Packs

Custom Surgical Packs, Manufactured to Your Facility's Exact Specification

SUBMED designs, assembles, and sterilizes custom procedure packs, surgical kits, and OR essentials for hospitals, surgery centers, and distributors — built to order, not off a shelf.

Founded 2010 Supplying 50+ Countries Custom & Standard Packs
Why choose SUBMED — manufacturing quality
Why Choose SUBMED

Manufacturing Precision, Backed by Global Reach

In-House Manufacturing

Packs and kits are designed, assembled, and quality-controlled by SUBMED — not sourced and resold from third-party catalogs.

Global Supply Experience

Established in 2010, supplying healthcare providers and distributors across 50+ countries.

Full Documentation on Request

Certificates and test reports across 19 international standards, including EN ISO 13485 and ISO 9001, available for procurement review. See our certifications

Standard or Fully Custom

Order from ready-to-ship standard packs, or configure a pack around your procedure, surgeon, or facility protocol.

What We Offer

Choose the Right Surgical Pack Program for Your Facility

Whether your facility needs a consistent, ready-to-ship pack or a fully configured program built around specific procedures and surgeons, SUBMED manufactures both in-house.

Standard Packs

Streamline supplies with packs that arrive complete and ready to use, manufactured to a consistent specification.

ConfigurationFixed, standard SKU
Typical lead timeProcessed within 1–5 business days
Minimum orderAsk your account contact
View Standard Packs
Our Process

From Specification to Sterile Shipment

1

Specify

We work from your preference card or facility standard to define pack contents.

2

Source

Materials and components are sourced against defined specifications.

3

Assemble

Packs are assembled in a controlled production environment.

4

Sterilize & Validate

Each batch is ethylene oxide sterilized (EN ISO 11135) and validated before release.

5

Ship

Packs are labeled with lot data and shipped per your facility's schedule.

Compliance & Documentation

What We Can Document for Procurement Review

FDA registered
FDA registered
ISO 13485 — Medical Device Quality Management System
ISO 13485Medical Device Quality Management System
ISO 11135 — Ethylene Oxide Sterilization
ISO 11135Ethylene Oxide Sterilization
ISO 14971 — Risk Management for Medical Devices
ISO 14971Risk Management for Medical Devices
IEC 62366-1 — Usability Engineering for Medical Devices
IEC 62366-1Usability Engineering for Medical Devices
ISO 9001 — Quality Management
ISO 9001Quality Management

Certificates and test reports are issued for specific sites, products, and revisions of each standard. See all certifications

SUBMED partnership
Ready to Connect?

Tell Us About Your Facility's Requirements

Complete the form and a member of our team will follow up directly — for a quote, a custom pack consultation, or a distributor partnership inquiry. No purchase required.

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Global Distribution

Export and international supply experience across multiple markets.

Documented Quality Process

Specifications and documentation available for procurement review.

Dedicated Account Support

A direct sales contact for quotes, reorders, and changes.

Custom Manufacturing Team

Standard configurations or packs built to your specification.