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Hai Laboratories, Inc.

Country not established FDA establishment FEI 3003046678

Devices
1
Registrations
FDA
FDA recalls
0

What Hai Laboratories, Inc. makes

HAI Laboratories, Inc. manufactures the CLINICAL SPECULAR MICROSCOPE, MODEL HAI CL-1000XYZ, which is a medical device used for clinical examinations.

The device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the US.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Company details

FDA FEI number
3003046678
Address
320 Massachusetts Ave, LEXINGTON, MA, 02420

Frequently asked questions

How many devices does HAI LABORATORIES, INC. have in the registry?

The registry currently lists 1 device for HAI LABORATORIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list HAI LABORATORIES, INC.'s devices?

Among its 1 most recently registered device, HAI LABORATORIES, INC. has devices listed in FDA 510(k) (1 device).

What risk classes do HAI LABORATORIES, INC.'s devices fall under?

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

What are the newest devices from HAI LABORATORIES, INC. in the registry?

The most recently registered devices listed for HAI LABORATORIES, INC. include CLINICAL SPECULAR MICROSCOPE, MODEL HAI CL-1000XYZ.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.