Skip to content

Biochem International, Inc.

United StatesFDA applicant, unverified

Devices
28

What Biochem International, Inc. makes

Biochem International, Inc. manufactures medical devices including oximeters (BIOCHEM MODEL 3301 NEWOX1 OXIMETER, BIOCHEM 3100 OXIMETER, BIOCHEM MICROSPAN 1040 OXIMETER), respiration monitors (BIOCHEM 515 RESPIRATION MONITOR), capnographs (BIOCHEM 8090 CAPNOGRAPH), transcutaneous oxygen monitors (MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT), muscle/tissue pH monitors (SENSOMAT MUSCLE/TISSUE PH), and blood pressure monitors (NON-INVASIVE, BLOOD PRESSURE MONITOR).

The company's portfolio includes Class I and Class II devices listed in the FDA 510(k) and FDA PMA registries. Biochem International, Inc. is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue28

Newest first, rows 1-28 of 28

Search and filter all 28 devices
Skip device list

Rows 1-28 of 28

Frequently asked questions

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

The registry currently lists 28 devices for Biochem International, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Biochem International, Inc.'s devices?

Among its 28 most recently registered devices, Biochem International, Inc. has devices listed in FDA 510(k) (27 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

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

Among its 28 most recently registered devices, the classes recorded for Biochem International, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Biochem International, Inc. include BIOCHEM MODEL 3301 NEWOX1 OXIMETER, BIOCHEM CO/OX 1000, MICRO SPAN TRANSCUTANEOUS OXYGEN MONIT and SENSOMAT.

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