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Micor, Inc.

United StatesFDA applicant, unverified

Devices
8

What Micor, Inc. makes

Micor, Inc. manufactures spring-wound epidural catheters, conduction catheters (including models like the Micor Conduction Cathéter and WundCath Conduction Cathéter), anesthesia conduction kits, angiography catheters, and percutaneous catheters designed for medical procedures requiring precise fluid or medication delivery.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are intended for use in the United States, where they are subject to compliance with FDA requirements for safety and performance.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue8

Newest first, rows 1-8 of 8

  • Spring-Wound Epidural Catheter Ref K991879

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Micor Conduction Catheter Ref K001717

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Wundcath Conduction Catheter Ref K003966

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Micor Anesthesia Conduction Kit Ref K001940

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Angiography Catheters Ref K854018

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Percutaneous Catheters Ref K860339

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Conduction Catheter Ref K031600

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Percutaneous Catheters Ref K861008

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Micor, Inc. have in the registry?

The registry currently lists 8 devices for Micor, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Micor, Inc.'s devices?

Among its 8 most recently registered devices, Micor, Inc. has devices listed in FDA 510(k) (8 devices).

What risk classes do Micor, Inc.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Micor, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Micor, Inc. in the registry?

The most recently registered devices listed for Micor, Inc. include SPRING-WOUND EPIDURAL CATHETER, MICOR CONDUCTION CATHETER, WUNDCATH CONDUCTION CATHETER and MICOR ANESTHESIA CONDUCTION KIT.

Generated automatically from registry data and not verified by a human reviewer.