Skip to content

Replacement Parts Industries, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000617661

Devices
3
Registrations
FDA
FDA recalls
0

What Replacement Parts Industries, Inc. makes

Replacement Parts Industries, Inc. manufactures phototherapy lights, skin or air temperature probes, and replacement heating elements for medical devices. These components are designed for use in therapeutic and monitoring equipment, including devices requiring precise temperature control or light-based treatments.

The company’s products are classified as Class II medical devices under FDA regulations and are supported by 510(k) clearances. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

Company details

FDA FEI number
1000617661
Address
625 Cochran St., Simi Valley, CA, 93065

Frequently asked questions

How many devices does REPLACEMENT PARTS INDUSTRIES, INC. have in the registry?

The registry currently lists 3 devices for REPLACEMENT PARTS INDUSTRIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list REPLACEMENT PARTS INDUSTRIES, INC.'s devices?

Among its 3 most recently registered devices, REPLACEMENT PARTS INDUSTRIES, INC. has devices listed in FDA 510(k) (3 devices).

What risk classes do REPLACEMENT PARTS INDUSTRIES, INC.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for REPLACEMENT PARTS INDUSTRIES, INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from REPLACEMENT PARTS INDUSTRIES, INC. in the registry?

The most recently registered devices listed for REPLACEMENT PARTS INDUSTRIES, INC. include RPI REPLACEMENT PHOTOTHERAPY LIGHTS, RPI SKIN OR AIR TEMPERATURE PROBE and RPI REPLACEMENT HEATING ELEMENTS.

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.