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Kleen Test Products Corporation

Also registered as Kleen Test Products

United Statesfrom the FDA registration address FDA establishment FEI 1526481

Devices
17
Registrations
FDA
FDA recalls
0

Catalogue17

Newest first, rows 1-17 of 17

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Rows 1-17 of 17

Company details

FDA FEI number
1526481
Address
216 12TH ST NE, Strasburg, OH, 44680

Frequently asked questions

How many devices does KLEEN TEST PRODUCTS CORPORATION have in the registry?

The registry currently lists 17 devices for KLEEN TEST PRODUCTS CORPORATION. Devices recorded under merged duplicate company entries are counted once.

Which registries list KLEEN TEST PRODUCTS CORPORATION's devices?

Among its 17 most recently registered devices, KLEEN TEST PRODUCTS CORPORATION has devices listed in FDA 510(k) (17 devices).

What risk classes do KLEEN TEST PRODUCTS CORPORATION's devices fall under?

Among its 17 most recently registered devices, the classes recorded for KLEEN TEST PRODUCTS CORPORATION's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from KLEEN TEST PRODUCTS CORPORATION in the registry?

The most recently registered devices listed for KLEEN TEST PRODUCTS CORPORATION include CAUTERY TIP CLEANING PAD, NEEDLE COUNTER-SURE COUNT/100 COUNT, SUTURE RACK & NEEDLE COUNTER and NEEDLE COUNTER-SURE COUNT/30 CT. MAGN..

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.