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Smith & Nephew, Mpl Division

Country not established

Devices
9

What Smith & Nephew, Mpl Division makes

The company manufactures single-use medical devices for procedural and injection applications, including hypodermic and spinal anesthesia needles, pressure syringes, heparin lock flush kits, and aspiration syringes. It also produces periodontal and endodontic probes, interosseous needles, and filter needles designed for intravenous use. Disposable dental and medical needles, along with related accessories, are part of the portfolio.

These devices are regulated under the FDA’s 510(k) pathway, with most classified as Class I or Class II. The portfolio appears in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Smith & Nephew, Mpl Division have in the registry?

The registry currently lists 9 devices for Smith & Nephew, Mpl Division. Devices recorded under merged duplicate company entries are counted once.

Which registries list Smith & Nephew, Mpl Division's devices?

Among its 9 most recently registered devices, Smith & Nephew, Mpl Division has devices listed in FDA 510(k) (9 devices).

What risk classes do Smith & Nephew, Mpl Division's devices fall under?

Among its 9 most recently registered devices, the classes recorded for Smith & Nephew, Mpl Division's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Smith & Nephew, Mpl Division in the registry?

The most recently registered devices listed for Smith & Nephew, Mpl Division include HYPO BRAND DISPOS. DENTAL NEEDLES-PLAST, HENKE JECT PRESSURE SYRINGE, MICRO Z DISPOS. SPINAL ANESTH. NEEDLE and HERAPIN LOCK FLUSH SOLUTION USE KIT.

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