Kleen Test Products Corporation
United Statesfrom the FDA registration address FDA establishment FEI 1526481
- Devices
- 17
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Search and filter all 17 devicesCompany 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..