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Adeza Biomedical

Country not established

Devices
3

What Adeza Biomedical makes

Adeza Biomedical makes the ROMCHECK specimen collection kit and the OBA(TM) serum hCG assay and OBA(TM) reader.

These devices are classified as Class I and Class II and are listed in the FDA 510(k) registry; the company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Romcheck Specimen Collection Kit Ref K900225 Open recall

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Oba(Tm) Serum Hcg Assay Ref K911047

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Oba(Tm) Reader Ref K911045

    Active Regimes: 510(k) Registry: 510(k) Class:I

Frequently asked questions

How many devices does Adeza Biomedical have in the registry?

The registry currently lists 3 devices for Adeza Biomedical. Devices recorded under merged duplicate company entries are counted once.

Which registries list Adeza Biomedical's devices?

Among its 3 most recently registered devices, Adeza Biomedical has devices listed in FDA 510(k) (3 devices).

What risk classes do Adeza Biomedical's devices fall under?

Among its 3 most recently registered devices, the classes recorded for Adeza Biomedical's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Adeza Biomedical in the registry?

The most recently registered devices listed for Adeza Biomedical include ROMCHECK SPECIMEN COLLECTION KIT, OBA(TM) SERUM HCG ASSAY and OBA(TM) READER.

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