# Sentinel Medical Technologies, LLC (manufacturer, Jacksonville, FL): 2 new FDA device listings, incl. intra-abdominal pressure monitoring device

**Score:** 80/100

| Field | Value |
|---|---|
| Establishment | Sentinel Medical Technologies, LLC |
| Role | Manufacturer |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device |
| Location | Jacksonville, FL, US |
| New listings | 2 |
| Devices | Intra-Abdominal Pressure Monitoring Device; Catheter, Retention Type, Balloon |
| Product codes | PHU, EZL |
| Device classes | Class II, Unclassified |
| Medical specialties | Gastroenterology, Urology |
| Brand names | TraumaGuard MindRay Cable, 000-0330; TraumaGuard Intra-abdominal Pressure System Catheter, 000-0221; TraumaGuard GE-Carescape Cable, 000-0320; TraumaGuard Spacelab cable, 000-0310; TraumaGuard Cable GE, 000-0260; TraumaGuard Cable Philips, 000-0250; TraumaGuard Universal Cable-R, 000-0290; TraumaGuard Nihon Koden Cable, 000-0280 |
| First new listing | 2026-09-21 |
| Latest new listing | 2026-09-21 |
| FDA registration number | 3021468326 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- U.S. establishment.
- Listed in the last 45 days.

Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) (https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRL/rl.cfm). Last refreshed: 2026-10-28T20:51:27.468Z.
From the openFDA device registration and listing data, refreshed weekly. A listing shows a device an establishment says it makes or handles for the U.S. market; it is not FDA clearance or approval. Contact persons and street addresses are not stored. Verify in the FDA Establishment Registration and Device Listing database.