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Medical Products Development, Inc.

United StatesFDA applicant, unverified

Devices
13

What Medical Products Development, Inc. makes

Medical Products Development, Inc. manufactures surgical cauteries and surgical lights, including reusable and disposable models for general and ophthalmic procedures. Their cautery devices feature temperature-controlled tips for precision tissue management, while their surgical lights provide adjustable brightness for operating room visibility. Examples include loop-tip cauteries for delicate microsurgery and battery-powered alternatives for portability.

All listed devices fall under FDA Class II regulation and are authorised via the 510(k) pathway. The company’s products are registered in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

Catalogue13

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  • Hi-Temp Surgical Cautery Ref K801323

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

  • Surg-Flex 5 Surgical Light Ref K810018

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

  • Multihi-Temp Cautery Ref K810015

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

  • Surg-Flex 15 Surgical Light Ref K810019

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

  • Hi-Temp Looptip Surgical Cautery Ref K802330

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

  • Perfectemp Ophthalmic Cautery Ref K801078

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

  • Hitemp. Tm 2 Looptip Cautery Ref K802942

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

  • Replacable Battery Hi-Temp Cautery Ref K810014

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

  • Microsurg Cautery Ref K810017

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

  • Replacable Battery Perfectemp Cautery Ref K810016

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

  • Multimicro Surgical Cautery Ref K810012

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

  • Surg-Flex 10 Light Ref K803067

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

  • Multiperfectemp Cautery Ref K810013

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

Rows 1-13 of 13

Frequently asked questions

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

The registry currently lists 13 devices for Medical Products Development, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medical Products Development, Inc.'s devices?

Among its 13 most recently registered devices, Medical Products Development, Inc. has devices listed in FDA 510(k) (13 devices).

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

Among its 13 most recently registered devices, the classes recorded for Medical Products Development, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Medical Products Development, Inc. include HI-TEMP SURGICAL CAUTERY, SURG-FLEX 5 SURGICAL LIGHT, MULTIHI-TEMP CAUTERY and SURG-FLEX 15 SURGICAL LIGHT.

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