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Spinalight, Inc.

United StatesFDA applicant, unverified

Devices
7

What Spinalight, Inc. makes

Spinalight, Inc. manufactures manual spinal adjusting instruments, including percussion tools, flexion distraction tables, and torque devices for spinal manipulation. Their portfolio includes models like the Atlas Percussion Adjusting Instrument, the Model 8000 Atlas C-1 Orthogonal Adjusting Instrument, and handheld adjustment tools. They also produce specialized tables, such as the Flexion Distraction Table and the HILO Table, designed for chiropractic and spinal therapy applications.

The company’s devices are classified under FDA categories Class I, Class II, and Unclassified (U), with many authorised via the 510(k) pathway. Their products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

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

The registry currently lists 7 devices for Spinalight, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Spinalight, Inc.'s devices?

Among its 7 most recently registered devices, Spinalight, Inc. has devices listed in FDA 510(k) (7 devices).

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

Among its 7 most recently registered devices, the classes recorded for Spinalight, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Spinalight, Inc. include Atlas Percussion Adjusting Instrument, MODELS 4100 AND 4300 MULTITHERAPY, MODEL 8000 ATLAS C-1 ORTHOGONAL ADJUSTING INSTRUMENT and FLEXION DISTRACTION TABLE.

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