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Olsen Electro-Surgical Instruments, Inc.

United StatesFDA applicant, unverified

Devices
3

What Olsen Electro-Surgical Instruments, Inc. makes

Olsen Electro-Surgical Instruments, Inc. manufactures disposable electro-surgical accessories, including holsters and switchpens designed for precision cutting and coagulation in surgical procedures. The holster (#770) is intended for securing and protecting electro-surgical tools, while the switchpens (#756, #757) are handheld devices used to control electro-cautery functions during operations.

The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) database, reflecting their compliance with US electro-surgical device standards. The manufacturer operates from the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does Olsen Electro-Surgical Instruments, Inc. have in the registry?

The registry currently lists 3 devices for Olsen Electro-Surgical Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Olsen Electro-Surgical Instruments, Inc.'s devices?

Among its 3 most recently registered devices, Olsen Electro-Surgical Instruments, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Olsen Electro-Surgical Instruments, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Olsen Electro-Surgical Instruments, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Olsen Electro-Surgical Instruments, Inc. in the registry?

The most recently registered devices listed for Olsen Electro-Surgical Instruments, Inc. include OLSEN #770 DISPOSABLE HOLSTER, DOUBLE-COAGULATION SWITCHPEN 757 and OLSEN 756 ROCKER SWITCHPEN.

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