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Laser Center Dev. Corp.

United StatesFDA applicant, unverified

Devices
2

What Laser Center Dev. Corp. makes

Laser Center Dev. Corp. manufactures the OCULOSTAT, a device used for stabilizing the eye during ocular procedures, and the AUTOMATED CORNEAL TREPHINE, a tool for precise corneal tissue cutting in surgical applications.

The company’s portfolio is regulated under Class I medical devices in the US, with devices listed via the FDA’s 510(k) pathway. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Oculostat Ref K981235

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

  • Automated Corneal Trephine Ref K981063

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

Frequently asked questions

How many devices does Laser Center Dev. Corp. have in the registry?

The registry currently lists 2 devices for Laser Center Dev. Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Laser Center Dev. Corp.'s devices?

Among its 2 most recently registered devices, Laser Center Dev. Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Laser Center Dev. Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Laser Center Dev. Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Laser Center Dev. Corp. in the registry?

The most recently registered devices listed for Laser Center Dev. Corp. include OCULOSTAT and AUTOMATED CORNEAL TREPHINE.

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