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The Olympus Optical Co.

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Devices
22

What The Olympus Optical Co. makes

The company manufactures flexible and reusable endoscopes, including bronchoscopes, colonoscopes, and cystoscopes, alongside disposable accessories like bending cannulas, biopsy forceps, and aspiration needles. Their portfolio also includes ultrasonic probes for female reproductive tract imaging, laryngofiberscopes with associated equipment, and video scopes for gastrointestinal procedures. Additional products encompass bronchoscopy balloon sheaths, tracheal intubation fiberscopes, and surgical systems such as the Sonosurg system for tissue ablation.

These devices are classified under FDA categories Class II and Unclassified (U), with most submissions supported by 510(k) clearances. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does The Olympus Optical Co. have in the registry?

The registry currently lists 22 devices for The Olympus Optical Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Olympus Optical Co.'s devices?

Among its 22 most recently registered devices, The Olympus Optical Co. has devices listed in FDA 510(k) (22 devices).

What risk classes do The Olympus Optical Co.'s devices fall under?

Among its 22 most recently registered devices, the classes recorded for The Olympus Optical Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Olympus Optical Co. in the registry?

The most recently registered devices listed for The Olympus Optical Co. include DISPOSABLE BENDING CANNULA PR-233Q, XBO1-824-18/19/20 BIOPSY FORCEPS, DISPOSABLE ASPIRATION NEEDLE NA-200H and ENDOSCOPE CONTOUR DETECTION DEVICE, MODEL 3DX45 AND COLONOSCOPE, MODEL XCF-Q140L/13D.

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