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C.B.S. Biotechnics, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
4

What C.B.S. Biotechnics, Inc. makes

C.B.S. Biotechnics, Inc. manufactures orthopedic fixation devices, including crystalline bone screws for endosseous applications, surgical instruments and accessories for orthopedic procedures, and the JSB Jet Syringe for medical injections. The company also produces the Endix Radicular Bioceramic Pin, designed for dental or orthopedic radicular stabilization.

The portfolio includes Class I and Class II devices, with products authorised via the FDA’s 510(k) pathway. These devices are listed under U.S. regulatory requirements, and the company operates from the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

Frequently asked questions

How many devices does C.B.S. Biotechnics, Inc. have in the registry?

The registry currently lists 4 devices for C.B.S. Biotechnics, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list C.B.S. Biotechnics, Inc.'s devices?

Among its 4 most recently registered devices, C.B.S. Biotechnics, Inc. has devices listed in FDA 510(k) (4 devices).

What risk classes do C.B.S. Biotechnics, Inc.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for C.B.S. Biotechnics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from C.B.S. Biotechnics, Inc. in the registry?

The most recently registered devices listed for C.B.S. Biotechnics, Inc. include CRYSTALLINE BONE SCREW ENDO-OSSEOUS, SURGICAL INSTRUMENTS & ACCESSORIES, JSB JET SYRINGE and ENDIX RADICULAR BIOCERAMIC PIN.

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