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Kenlor Industries, Inc.

Country not established FDA establishment FEI 2027370

Devices
9
Registrations
FDA
FDA recalls
0

What Kenlor Industries, Inc. makes

Kenlor Industries, Inc. manufactures liquid controls for urine and spinal fluid testing, as well as assay kits for measuring iron levels, microproteins, total protein, and *Helicobacter pylori* antibodies. Their products include therapeutic drug monitoring controls and reagents for laboratory diagnostics.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions recorded in the FDA’s 510(k) clearance registry. These products are intended for in vitro diagnostic use and are listed in the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

Company details

FDA FEI number
2027370
Address
1560 EAST EDINGER AVE., SANTA ANA, CA, 92705

Frequently asked questions

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

The registry currently lists 9 devices for KENLOR INDUSTRIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list KENLOR INDUSTRIES, INC.'s devices?

Among its 9 most recently registered devices, KENLOR INDUSTRIES, INC. has devices listed in FDA 510(k) (9 devices).

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

Among its 9 most recently registered devices, the classes recorded for KENLOR INDUSTRIES, INC.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for KENLOR INDUSTRIES, INC. include KENLOR LIQUID TOTAL URINE CONTROL, KENLOR LIQUID URINE CONTROL, KENLOR HUMAN SPINAL FLUID CONTROL and KENLOR TOTAL IRON, UIBC/TIBC ASSAY KIT.

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.