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Precision Corneal Instruments

Country not established

Devices
1

What Precision Corneal Instruments makes

Precision Corneal Instruments manufactures ultrasonic pachymeters, which measure corneal thickness using high-frequency sound waves for diagnostic and preoperative assessments in ophthalmology.

The company’s devices are classified as Class II under FDA regulations and are listed via the 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.

Catalogue1

Newest first, rows 1-1 of 1

  • Ultrasonic Pachymeter Ref K921705

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

Frequently asked questions

How many devices does Precision Corneal Instruments have in the registry?

The registry currently lists 1 device for Precision Corneal Instruments. Devices recorded under merged duplicate company entries are counted once.

Which registries list Precision Corneal Instruments's devices?

Among its 1 most recently registered device, Precision Corneal Instruments has devices listed in FDA 510(k) (1 device).

What risk classes do Precision Corneal Instruments's devices fall under?

Among its 1 most recently registered device, the classes recorded for Precision Corneal Instruments's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Precision Corneal Instruments in the registry?

The most recently registered devices listed for Precision Corneal Instruments include ULTRASONIC PACHYMETER.

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