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Tetrous, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3029780995

Devices
13
Registrations
FDA
FDA recalls
0

Catalogue13

Newest first, rows 1-13 of 13

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Rows 1-13 of 13

Company details

FDA FEI number
3029780995
Address
2021 Midwest Rd Ste 101, Oak Brook, IL, 60523

Frequently asked questions

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

The registry currently lists 13 devices for TETROUS, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list TETROUS, INC.'s devices?

Among its 13 most recently registered devices, TETROUS, INC. has devices listed in FDA GUDID (13 devices).

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

Among its 13 most recently registered devices, the classes recorded for TETROUS, INC.'s devices are Class I. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for TETROUS, INC. include Introducer Probe - Flat Collar TET-INS-005, Introducer Probe - Stepped Collar TET-INS-004, Awl - Non-Cutting TET-INS-011 and Cutting Awl - 5.5mm TET-INS-012.

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.