Skip to content

Richard'S Medical Equip., Inc.

United StatesFDA applicant, unverified

Devices
48

What Richard'S Medical Equip., Inc. makes

Richard’s Medical Equip., Inc. manufactures orthopedic and otology devices, including femoral prostheses, fracture frames, and drainage tubes. Their portfolio includes cement restrictors for orthopedic procedures, titanium ventilated tubes, and plastic pore plugs for surgical applications. Specialized items like a clavicle strap, ribbons for otology, and modified Teflon pistons are also produced.

The company’s devices are regulated under FDA 510(k) clearance, with products classified as Class I and Class II. These items are listed in the FDA’s 510(k) registry. The manufacturer operates in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue48

Newest first, rows 1-48 of 48

Search and filter all 48 devices
Skip device list

Rows 1-48 of 48

Frequently asked questions

How many devices does Richard'S Medical Equip., Inc. have in the registry?

The registry currently lists 48 devices for Richard'S Medical Equip., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Richard'S Medical Equip., Inc.'s devices?

Among its 48 most recently registered devices, Richard'S Medical Equip., Inc. has devices listed in FDA 510(k) (48 devices).

What risk classes do Richard'S Medical Equip., Inc.'s devices fall under?

Among its 48 most recently registered devices, the classes recorded for Richard'S Medical Equip., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Richard'S Medical Equip., Inc. in the registry?

The most recently registered devices listed for Richard'S Medical Equip., Inc. include PLUG-LOK CEMENT RESTIRCTOR, SPECTRON PRIMARY STEM FEMORAL PROSTHES, REUTER BOBBIN VENTILA. TUBE-TITANIUM and PULLEN PLASTIC-PORE PLUGS.

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