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Wells Johnson Co.

United Statesfrom the FDA registration address FDA establishment FEI 2024022

Devices
15
Registrations
FDA
FDA recalls
0

What Wells Johnson Co. makes

Wells Johnson Co. manufactures a range of medical devices including fixation systems, various suction tips and aspirators, external mechanical fasteners, endoscopic systems with fiber optic illumination, an ultrasonic aspirator system, and an infusion system model 20-6000-00.

These products fall under Class I, Class II, and U classifications and are listed in the FDA 510(k) registry; the company is based in the United States.

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

Catalogue15

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Company details

FDA FEI number
2024022
Address
8000 S Kolb Rd, Tucson, AZ, 85756

Frequently asked questions

How many devices does WELLS JOHNSON CO. have in the registry?

The registry currently lists 15 devices for WELLS JOHNSON CO.. Devices recorded under merged duplicate company entries are counted once.

Which registries list WELLS JOHNSON CO.'s devices?

Among its 15 most recently registered devices, WELLS JOHNSON CO. has devices listed in FDA 510(k) (15 devices).

What risk classes do WELLS JOHNSON CO.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for WELLS JOHNSON CO.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from WELLS JOHNSON CO. in the registry?

The most recently registered devices listed for WELLS JOHNSON CO. include WELLS JOHNSON FIXATION SYSTEM, PLASTIC SUCTION TIPS, WELLS JOHNSON WECO MONOPOLAR/FRAZIER SUCTION PROBE and EXTERNAL MECHANICAL FASTENER.

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.