510(k) Report

FDA applicant

Vital Connections, Inc.

Tipp City, OH2 decisions1988–19970 recalls

FDA records 2 decisions for Vital Connections, Inc. (Tipp City, OH) from 1988 to 1997: 2 510(k) clearances. Most are in product codes DSA (Cable, Transducer And Electrode, Patient…) and DRX (Electrode, Electrocardiograph). 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, cardiovascular panel, where it files most

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

FDA decisions per year

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

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Vital Connections, 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.