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Sandal Surgico

PakistanFDA applicant, unverified

Devices
1

What Sandal Surgico makes

Sandal Surgico manufactures percussion hammers, tools designed for orthopedic and surgical applications to assist in bone manipulation and reduction procedures.

The company’s percussion hammer is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The manufacturer is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Percussion Hammer Ref K891571

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

Frequently asked questions

How many devices does Sandal Surgico have in the registry?

The registry currently lists 1 device for Sandal Surgico. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sandal Surgico's devices?

Among its 1 most recently registered device, Sandal Surgico has devices listed in FDA 510(k) (1 device).

What risk classes do Sandal Surgico's devices fall under?

Among its 1 most recently registered device, the classes recorded for Sandal Surgico's devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Sandal Surgico in the registry?

The most recently registered devices listed for Sandal Surgico include PERCUSSION HAMMER.

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