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Steritec Products Mfg. Co., Inc.

United Statesfrom the FDA registration address FDA establishment FEI 1000125215

Devices
22
Registrations
FDA
FDA recalls
0

Catalogue22

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Company details

FDA FEI number
1000125215
Address
74 INVERNESS DR E, Englewood, CO, 80112

Frequently asked questions

How many devices does STERITEC PRODUCTS MFG. CO., INC. have in the registry?

The registry currently lists 22 devices for STERITEC PRODUCTS MFG. CO., INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list STERITEC PRODUCTS MFG. CO., INC.'s devices?

Among its 22 most recently registered devices, STERITEC PRODUCTS MFG. CO., INC. has devices listed in FDA 510(k) (22 devices).

What risk classes do STERITEC PRODUCTS MFG. CO., INC.'s devices fall under?

Among its 22 most recently registered devices, the classes recorded for STERITEC PRODUCTS MFG. CO., INC.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from STERITEC PRODUCTS MFG. CO., INC. in the registry?

The most recently registered devices listed for STERITEC PRODUCTS MFG. CO., INC. include STERITEC GREEN CARD PACK BOWIE-DICK TEST, EMU-GRAPH EMULATOR, MODEL CI 131, STERI-PAK BOWIE DICK TEST PACK and STERITEC CROSS-CHECKS EO GAS STERILIZATION INTEGRATOR.

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.