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Catachem, Inc.

United StatesFDA applicant, unverified FDA FEI 2434178

Devices
42
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

Catalogue42

Newest first, rows 1-42 of 42

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Rows 1-42 of 42

Company details

FDA FEI number
2434178
DUNS number
109130625
Address
353 Christian St Ste 2, Oxford, CT, 06478
Phone
203-262-0330

Frequently asked questions

How many devices does Catachem, Inc. have in the registry?

The registry currently lists 42 devices for Catachem, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Catachem, Inc.'s devices?

Among its 42 most recently registered devices, Catachem, Inc. has devices listed in FDA 510(k) (41 devices) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Catachem, Inc.'s devices fall under?

Among its 42 most recently registered devices, the classes recorded for Catachem, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Catachem, Inc. in the registry?

The most recently registered devices listed for Catachem, Inc. include ALANINE AMINOTRANSFERASE (ALT)/(GPT), ASPARTATE AMINOTRANSFERASE (AST)/(GOT), Catachem DiscretPak™ C402-0C and UIBC FOR DISCREET RANDOM ACCESS ANALYZER.

Generated automatically from registry data and not verified by a human reviewer.