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Escalon Trek Medical

Country not established

Devices
3

What Escalon Trek Medical makes

Escalon Trek Medical produces medical devices including viscous fluid systems for surgical applications, the VITLITE (TR7700) surgical light system, and the Autopole regulator system for managing gas flow in medical procedures.

These devices are regulated under FDA 510(k) clearance, with classifications spanning Class I and Class II. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Viscous Fluid System Ref K963434

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Vitlite (TR7700) Ref K963417

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Autopole Regulator System Ref K924999

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

Frequently asked questions

How many devices does Escalon Trek Medical have in the registry?

The registry currently lists 3 devices for Escalon Trek Medical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Escalon Trek Medical's devices?

Among its 3 most recently registered devices, Escalon Trek Medical has devices listed in FDA 510(k) (3 devices).

What risk classes do Escalon Trek Medical's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Escalon Trek Medical's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Escalon Trek Medical in the registry?

The most recently registered devices listed for Escalon Trek Medical include VISCOUS FLUID SYSTEM, VITLITE (TR7700) and AUTOPOLE REGULATOR SYSTEM.

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