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M.B. Industries, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
3

What M.B. Industries, Inc. makes

M.B. Industries, Inc. manufactures ophthalmic surgical instruments, specifically co-axial illuminated retinal picks, fiberoptic endo-illuminators, and standard illuminated retinal picks.

These Class II medical devices are listed in the FDA 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

Frequently asked questions

How many devices does M.B. Industries, Inc. have in the registry?

The registry currently lists 3 devices for M.B. Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list M.B. Industries, Inc.'s devices?

Among its 3 most recently registered devices, M.B. Industries, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do M.B. Industries, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for M.B. Industries, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from M.B. Industries, Inc. in the registry?

The most recently registered devices listed for M.B. Industries, Inc. include MBI CO-AXIAL ILLUMINATED RETINAL PICK, MBI FIBEROPTIC ENDO-ILLUMINATOR and MBI ILLUMINATED RETINAL PICK.

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