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Servo Med, Inc.

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Devices
1

What Servo Med, Inc. makes

Servo Med, Inc. manufactures the NYSTAGMOGRAPH NG-1, a device used for assessing vestibular function by recording eye movements during nystagmus testing. This equipment supports clinical evaluation of balance disorders and inner ear pathologies.

The NYSTAGMOGRAPH NG-1 is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Servo Med Nystagmograph Ng-1 Ref K843004

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

Frequently asked questions

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

The registry currently lists 1 device for Servo Med, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Servo Med, Inc.'s devices?

Among its 1 most recently registered device, Servo Med, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Servo Med, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Servo Med, Inc. include SERVO MED NYSTAGMOGRAPH NG-1.

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