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Medical Products Laboratories, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 2513595

Devices
26
Registrations
FDA
FDA recalls
0

What Medical Products Laboratories, Inc. makes

Medical Products Laboratories, Inc. manufactures dental and orthodontic products, including the Pre-Klene Enamel Cleaner—a solution for preparing tooth surfaces—and VarnishAmerica, a protective coating applied to teeth.

These products are regulated under FDA’s Class I and Class II categories, with some requiring 510(k) clearance. They are listed in the FDA’s 510(k) database. The company is based in the United States.

AI-generated from registry data, 4 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Company details

FDA FEI number
2513595
Address
9990 Global Rd, Philadelphia, PA, 19115

Frequently asked questions

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

The registry currently lists 26 devices for MEDICAL PRODUCTS LABORATORIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list MEDICAL PRODUCTS LABORATORIES, INC.'s devices?

Among its 26 most recently registered devices, MEDICAL PRODUCTS LABORATORIES, INC. has devices listed in FDA 510(k) (2 devices) and FDA GUDID (24 devices). A device can be listed in more than one registry, so these counts overlap.

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

Among its 26 most recently registered devices, the classes recorded for MEDICAL PRODUCTS LABORATORIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for MEDICAL PRODUCTS LABORATORIES, INC. include VarnishAmerica 00007, VarnishAmerica 00008, VarnishAmerica 00006 and VarnishAmerica 00013.

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.