Skip to content

Smr

Country not established

Devices
2

What Smr makes

Smr manufactures the SMR Paragon Chair Table, a medical table designed for patient positioning and support in clinical settings, and the Dimension I Refraction System, an optical device used for eye examinations and vision correction assessments.

The company’s products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. These devices are based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Smr Paragon Chair Table Ref K811623

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Dimension I Refraction System Ref K801767

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

Frequently asked questions

How many devices does Smr have in the registry?

The registry currently lists 2 devices for Smr. Devices recorded under merged duplicate company entries are counted once.

Which registries list Smr's devices?

Among its 2 most recently registered devices, Smr has devices listed in FDA 510(k) (2 devices).

What risk classes do Smr's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Smr's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Smr in the registry?

The most recently registered devices listed for Smr include SMR PARAGON CHAIR TABLE and DIMENSION I REFRACTION SYSTEM.

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