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Lsi Intl., Inc.

United StatesFDA applicant, unverified

Devices
5

What Lsi Intl., Inc. makes

Lsi Intl., Inc. manufactures spinal traction and decompression devices, including the S.P. 100, Quantum Intersegmental Traction Table models 400, 401, 400H, and 401H, and the MS400, MS 2500, and MS300 units.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

  • S.P. 100 Ref K970696

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Quantum Intersegmental Traction Table 400, 401, 400H, 401H Ref K002390

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • MS400 Ref K984113

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Ms 2500 Ref K933653

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • MS300 Ref K984021

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

Frequently asked questions

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

The registry currently lists 5 devices for Lsi Intl., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lsi Intl., Inc.'s devices?

Among its 5 most recently registered devices, Lsi Intl., Inc. has devices listed in FDA 510(k) (5 devices).

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

Among its 5 most recently registered devices, the classes recorded for Lsi Intl., Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Lsi Intl., Inc. include S.P. 100, QUANTUM INTERSEGMENTAL TRACTION TABLE 400, 401, 400H, 401H, MS400 and MS 2500.

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