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Adaptive Switch Laboratories, Inc.

Country not established FDA establishment FEI 1000118602

Devices
4
Registrations
FDA
FDA recalls
0

What Adaptive Switch Laboratories, Inc. makes

Adaptive Switch Laboratories, Inc. manufactures assistive technology devices, including the ASL Model #104, ASL Model #102, ASL Model 101, and ASL Model #103, which are designed to support individuals with disabilities in accessing communication and environmental controls.

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, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Asl Model #104 Ref K914737

    Class II
    Active 510(k) 510(k) II
  • Asl Model #102 Ref K914739

    Class II
    Active 510(k) 510(k) II
  • Asl Model 101 Ref K914738

    Class II
    Active 510(k) 510(k) II
  • Asl Model #103 Ref K914740

    Class II
    Active 510(k) 510(k) II

Company details

FDA FEI number
1000118602
Address
125 SPUR 191, SUITE C, SPICEWOOD, TX, 78669

Frequently asked questions

How many devices does ADAPTIVE SWITCH LABORATORIES, INC. have in the registry?

The registry currently lists 4 devices for ADAPTIVE SWITCH LABORATORIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list ADAPTIVE SWITCH LABORATORIES, INC.'s devices?

Among its 4 most recently registered devices, ADAPTIVE SWITCH LABORATORIES, INC. has devices listed in FDA 510(k) (4 devices).

What risk classes do ADAPTIVE SWITCH LABORATORIES, INC.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for ADAPTIVE SWITCH LABORATORIES, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from ADAPTIVE SWITCH LABORATORIES, INC. in the registry?

The most recently registered devices listed for ADAPTIVE SWITCH LABORATORIES, INC. include ASL MODEL #104, ASL MODEL #102, ASL MODEL 101 and ASL MODEL #103.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.