FDA-Regulated Medical Device Catalog

Complete portfolio of Veridian Corp medical devices with 510(k) numbers, classification, and regulatory detail pages

5
Active Devices
3
510(k) Cleared
4
Class II Devices
1
Pending Submission

Device Master Record

Each device has a dedicated regulatory detail page at a URL containing the 510(k) number for scraper path-based data extraction testing.

Model Device Name Class 510(k) / Pathway Product Code CFR Regulation UDI-DI Status Detail URL
VPM-4000 Veridian Pulse Monitor II K240847 DRT 21 CFR 870.2340 00842684701234 Marketed View →
VGP-200 Veridian Glucose Patch II K231156 NBW 21 CFR 862.1355 00842684702345 Marketed View →
VID-100 Veridian Insulin Delivery System II K220893 FRN 21 CFR 880.5730 00842684703456 Marketed View →
VT-50 Veridian Clinical Thermometer I Exempt (Listing) FLL 21 CFR 880.2910 00842684704567 Marketed —
VBC-300 Veridian BP Cuff System II K26XXXX (Pending) DXN 21 CFR 870.1130 — Pre-Submission —

Device Detail Pages (URL-Embedded Regulatory Data)

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Veridian Pulse Monitor

510(k) K240847 · Class II · Cardiovascular panel · Continuous ECG monitoring

URL: /regulatory/devices/veridian-pulse-monitor-k240847.html
🩸

Veridian Glucose Patch

510(k) K231156 · Class II · Clinical Chemistry · Continuous glucose monitoring

URL: /regulatory/devices/veridian-glucose-patch-k231156.html
💉

Veridian Insulin Delivery System

510(k) K220893 · Class II · General Hospital · Automated insulin delivery

URL: /regulatory/devices/veridian-insulin-pump-k220893.html

Manufacturing & Distribution Sites

Site ID Location FEI Number Devices Manufactured FDA Registration
MFG-SF-001 1200 Innovation Drive, San Francisco, CA 94107 3012345678 VPM-4000, VGP-200, VT-50 Active
MFG-AUS-002 8400 Tech Ridge Blvd, Austin, TX 78753 3012345679 VID-100, VBC-300 Active
DIST-CHI-003 500 Commerce Street, Chicago, IL 60654 3012345680 All devices (distribution only) Active