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Optek Medico Co., Ltd.

Country not established

Devices
3

What Optek Medico Co., Ltd. makes

Optek Medico Co., Ltd. manufactures slit lamp models (OPM SLIT LAMP Model P-1 and Model P-3) and triamcinolone acetonide (TIA) lens sets for ophthalmic examinations and procedures.

These devices are regulated under FDA 510(k) clearance, with slit lamps classified as Class II and the TIA lens set as Class I. The company is based in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Opm Slit Lamp Model P-1 & Model P-3 Ref K863048

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Opm Slit Lamp Model P-1 Ref K861854

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Tria Lens Set Ref K843095

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

Frequently asked questions

How many devices does Optek Medico Co., Ltd. have in the registry?

The registry currently lists 3 devices for Optek Medico Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Optek Medico Co., Ltd.'s devices?

Among its 3 most recently registered devices, Optek Medico Co., Ltd. has devices listed in FDA 510(k) (3 devices).

What risk classes do Optek Medico Co., Ltd.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Optek Medico Co., Ltd.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Optek Medico Co., Ltd. in the registry?

The most recently registered devices listed for Optek Medico Co., Ltd. include OPM SLIT LAMP MODEL P-1 & MODEL P-3, OPM SLIT LAMP MODEL P-1 and TRIA LENS SET.

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