Skip to content

Sierra Surgical, Inc.

Country not established

Devices
1

What Sierra Surgical, Inc. makes

Sierra Surgical, Inc. manufactures the TEMPERLITE(TM) SAW BLADE, which is a Class II medical device.

The company is based in the US and its devices are listed in the FDA 510(k) registry.

AI-generated from registry data, 23 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Temperlite(Tm) Saw Blade Ref K911902

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

Frequently asked questions

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

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

Which registries list Sierra Surgical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Sierra Surgical, Inc. include TEMPERLITE(TM) SAW BLADE.

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