FDA applicant

Metra Biosystems, Inc.

Laurel, MD7 decisions1995–19981 recall

FDA records 7 decisions for Metra Biosystems, Inc. (Laurel, MD) from 1995 to 1998: 7 510(k) clearances. Most are in product codes JMM (Column Chromatography & Color Development…) and CIN (Electrophoretic Separation, Alkaline…). 1 recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Metra Biosystems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Metra Biosystems, Inc. since 2007.

Recalls per year

1in 2016

2007high 1 (2016) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Metra Biosystems, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Metra Biosystems, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?