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

Sentinel Medical Technologies, LLC (Jacksonville, Florida): 2 new FDA device listings, incl. intra-abdominal pressure monitoring device. Its amount of 2 is above the median of 1 (69th percentile). Dated 44 days ago, it serves as a historical benchmark. Score 80/100. As of 2026-10-28, from openFDA device registration and listing endpoint (U.S. Food and Drug Administration).

Data as of · Compiled by Zalwin from openFDA device registration and listing endpoint (U.S. Food and Drug Administration)

amount: 2 · 69th percentile of 2,570 DeviceEstablishmentPulse records · 2.0x the median

Free preview: all 14 published fields of this record are shown below. Locked: 83 related FL DeviceEstablishmentPulse records and the 5-column CSV export.

FieldValue
EstablishmentSentinel Medical Technologies, LLC
RoleManufacturer
Establishment typesComplaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility; Manufacture Medical Device
LocationJacksonville, FL, US
New listings2
DevicesIntra-Abdominal Pressure Monitoring Device; Catheter, Retention Type, Balloon
Product codesPHU, EZL
Device classesClass II, Unclassified
Medical specialtiesGastroenterology, Urology
Brand namesTraumaGuard 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 listing2026-09-21
Latest new listing2026-09-21
FDA registration number3021468326
Registration expires2026-12-31
amount percentile69th of 2,570 (median 1, 2.0x median)
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CSV columns: Establishment · Role · New listings · Devices · Latest listing · official source URL

  • Source agency: openFDA device registration and listing endpoint (U.S. Food and Drug Administration)
  • Record date: 2026-09-21
  • Data refreshed: 2026-10-28
  • Refunds on request within 14 days

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LIVE PUBLIC DATA Source: openFDA device registration and listing endpoint (U.S. Food and Drug Administration) · Last refreshed: Wed, 28 Oct 2026 20:51:27 GMT

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Peer benchmark and outreach value: Sentinel Medical Technologies, LLC and 84 Florida peers

  • Florida DeviceEstablishmentPulse records like this one: 84
  • Sentinel Medical Technologies, LLC's amount: 69th percentile of 2,570 records
  • Timing: Low: older than 30 days
  • Estimated pipeline if you contact every Florida peer: $16,800 (peers × rate × deal size; an estimate from your assumptions, not a forecast)

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80 / 100 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.

What is the DeviceEstablishmentPulse record for Sentinel Medical Technologies, LLC in Jacksonville, Florida?

Sentinel Medical Technologies, LLC (Jacksonville, FL), a manufacturer, added 2 FDA device listings on 2026-09-21.

How does Sentinel Medical Technologies, LLC compare to other Florida DeviceEstablishmentPulse records?

Its amount of 2 sits in the upper half (69th percentile) of 2,570 records; the median is 1. It is 44 days old, still within a typical 45-day follow-up window. Its Score of 80/100 puts it among the stronger signals in this feed.

Sentinel Medical Technologies, LLC vs. top 3 peers

OrganizationLocationAmountPercentileRecord date
Sentinel Medical Technologies, LLCJacksonville, FL269th2026-09-21
Beacon Biosignals, Inc.Boston, MA377th2026-10-16
Endovascular Engineering, Inc.Menlo Park, CA377th2026-10-14
INNO Holdings Inc.Millcreek, UT377th2026-10-05

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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.

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