FDA applicant

Vital Metrics, Inc.

San Diego, CA9 decisions1982–19880 recalls

FDA records 9 decisions for Vital Metrics, Inc. (San Diego, CA) from 1982 to 1988: 9 510(k) clearances. Most are in product codes FFG (Device, Urine Flow Rate Measuring…) and KNX (Collector, Urine, (And Accessories) For…). No 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Vital Metrics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Vital”

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

Vital Signs, Inc. 75 Vital Images, Inc. 41 Vital Scientific N.V. 5 Vital Diagnostics (Manufacturing) Ptyltd 5 Vital Concepts, Inc. 4 Vital Connections, Inc. 2 Vital Art and Science Incorporated 2 Vital Signs, Inc., A GE Healthcare Company 2 Vital Access 1 Vital Signs Colorado, Inc. 1 Vital Flow Products Corp. 1 Vital 5 1

Vital Metrics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vital”