FDA applicant

Biometric Research Institute, Inc.

Arlington, VA2 decisions1991–19911 recall

FDA records 2 decisions for Biometric Research Institute, Inc. (Arlington, VA) in 1991: 2 510(k) clearances. Most are in product codes DXG (Computer, Diagnostic, Pre-Programmed…) and KRB (Probe, Thermodilution). 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, cardiovascular panel, where it files most

How often FDA has decided Biometric Research Institute, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Biometric Research Institute, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Biometric Research Institute, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Biometric”

FDA records each applicant name separately; these may or may not be the same firm.

Biometric Products, Inc. 5 Biometric Analysis Group, Inc. 2

Biometric Research Institute, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Biometric”