Vitalconnect, Inc.
Vitalconnect, Inc. holds FDA 510(k) medical device clearances, first cleared 2014, most recent 2025, with 1 FDA device recall on record.
Top product codes for Vitalconnect, Inc.
FDA recalls by Vitalconnect, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Vitalconnect, Inc.
- K242129 — VitalRhythm
- K193343 — Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)
- K192757 — VitalPatch 5D Biosensor - single, VitalPatch 7D Biosensor - single, VitalPatch 5D Biosensor bag of 20, VitalPatch 7D Biosensor bag of 20
- K190916 — VitalPatch 7D Biosensor - single, VitalPatch 7D Biosensor - bag of 20
- K183078 — VitalConnect Platform, VitalPatch Biosensor
- K163453 — VitalPatch® VitalConnect Platform
- K170973 — VitalWatch Software User Interface
- K152139 — Vital Connect Platform, HealthPatch MD, VitalPatch
- K141167 — VITALCONNECT PLATFORM (CONSISTING OF VITALCONNECT SENSOR, RELAY SOFTWARE LIBRARY AND SECURE SERVER SOFTWARE LIBRARY)
- K132447 — VITALCONNECT PLATFORM BY VITAL CONNECT INC.
Data sourced from openFDA. This site is unofficial and independent of the FDA.