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Micropoint Technologies Pte, Ltd.

SingaporeFDA applicant, unverified

Devices
1

What Micropoint Technologies Pte, Ltd. makes

Micropoint Technologies manufactures the PLANCET, a medical device designed for precise tissue analysis and biopsy procedures, enabling accurate sampling of lesions or abnormal tissue.

The PLANCET is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Plancet Ref K113513

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

Frequently asked questions

How many devices does Micropoint Technologies Pte, Ltd. have in the registry?

The registry currently lists 1 device for Micropoint Technologies Pte, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Micropoint Technologies Pte, Ltd.'s devices?

Among its 1 most recently registered device, Micropoint Technologies Pte, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Micropoint Technologies Pte, Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Micropoint Technologies Pte, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Micropoint Technologies Pte, Ltd. in the registry?

The most recently registered devices listed for Micropoint Technologies Pte, Ltd. include PLANCET.

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