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Avec Scientific Design Corp.

United StatesFDA 510(k) applicant, unverified

Devices
6

What Avec Scientific Design Corp. makes

Avec Scientific Design Corp. manufactures orthopedic and spinal surgical accessories, including the Kambin laminectomy frame for spinal procedures, an irrigation pressure monitor for surgical fluid control, and a bilateral continuous passive motion device for postoperative rehabilitation. Their product line also covers spinal stabilization tools like the Chop spine frame and a tourniquet pressure regulator for limb isolation during surgery. Additional items include an over-drape leg holder for patient positioning.

The company’s devices are classified under FDA categories Class I and Class II, with regulatory submissions recorded in the FDA’s 510(k) clearance database. Their products are listed under U.S. jurisdiction, and the manufacturer is based in the United States.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Avec Scientific Design Corp. have in the registry?

The registry currently lists 6 devices for Avec Scientific Design Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Avec Scientific Design Corp.'s devices?

Among its 6 most recently registered devices, Avec Scientific Design Corp. has devices listed in FDA 510(k) (6 devices).

What risk classes do Avec Scientific Design Corp.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Avec Scientific Design Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Avec Scientific Design Corp. in the registry?

The most recently registered devices listed for Avec Scientific Design Corp. include KAMBIN LAMINECTOMY FRAME, IRRIGATION PRESSURE MONITOR, BILATERAL CONTINUOUS PASSIVE MOTION DEVICE and CHOP SPINE FRAME.

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