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Mnlase, Inc.

United StatesFDA applicant, unverified

Devices
22

What Mnlase, Inc. makes

Mnlase, Inc. manufactures laser delivery probes and endoscopic photocoagulator lasers, including curved and aspirating models such as the CURVD ENDOPHOTOCOAGULATOR LASER PROBE, ORS series devices, and various MODEL-series probes like the 230-SAS, 220-SC, 130-SAC, 220-SS, 120-SC, and 210-AS.

These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue22

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Frequently asked questions

How many devices does Mnlase, Inc. have in the registry?

The registry currently lists 22 devices for Mnlase, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Mnlase, Inc.'s devices?

Among its 22 most recently registered devices, Mnlase, Inc. has devices listed in FDA 510(k) (22 devices).

What risk classes do Mnlase, Inc.'s devices fall under?

Among its 22 most recently registered devices, the classes recorded for Mnlase, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Mnlase, Inc. in the registry?

The most recently registered devices listed for Mnlase, Inc. include CURVD ENDOPHOTOCOGULATOR LASER PROBE, ORS-300, ORS-2000 SERIES and ORS-1000.

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