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Power Products, Inc.-Splintek

United StatesFDA applicant, unverified

Devices
3

What Power Products, Inc.-Splintek makes

Power Products, Inc.-Splintek manufactures orthopedic splinting devices, including the EZ SPLINT and EZ SPLINT PM for immobilizing fractures or injuries, as well as the SLEEP RIGHT series (Select, Low Profile, and Advance) for nighttime wrist or forearm support.

These devices are classified as Class II under FDA regulations and are listed via 510(k) clearance. The company 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

  • Ez Splint & Ez Splint Pm Ref K022809

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Sleep Right - Select, Low Profile And Advance Ref K071404

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Sleepright Ref K100545

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

Frequently asked questions

How many devices does Power Products, Inc.-Splintek have in the registry?

The registry currently lists 3 devices for Power Products, Inc.-Splintek. Devices recorded under merged duplicate company entries are counted once.

Which registries list Power Products, Inc.-Splintek's devices?

Among its 3 most recently registered devices, Power Products, Inc.-Splintek has devices listed in FDA 510(k) (3 devices).

What are the newest devices from Power Products, Inc.-Splintek in the registry?

The most recently registered devices listed for Power Products, Inc.-Splintek include EZ SPLINT & EZ SPLINT PM, SLEEP RIGHT - SELECT, LOW PROFILE AND ADVANCE and SLEEPRIGHT.

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