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Sapphire Medical, Inc.

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Devices
1

What Sapphire Medical, Inc. makes

Sapphire Medical, Inc. manufactures the CINCH BONE ANCHOR SYSTEM, a spinal fixation device designed for securing intervertebral implants or bone grafts during surgical procedures.

The CINCH BONE ANCHOR SYSTEM is classified as a Class II medical device in the U.S. and is listed under the FDA’s 510(k) pathway. 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

  • Cinch Bone Anchor System Ref K062739

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

Frequently asked questions

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

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

Which registries list Sapphire Medical, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Sapphire Medical, Inc. include CINCH BONE ANCHOR SYSTEM.

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