# Rsi Technology Group, LLC (specification developer, Frisco, TX): 2 new FDA device listings, incl. container, specimen, sterile

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Rsi Technology Group, LLC |
| Owner / operator | RSI Technology Group, LLC |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Develop Specifications But Do Not Manufacture At This Facility |
| Location | Frisco, TX, US |
| New listings | 2 |
| Devices | Container, Specimen, Sterile; Container, Specimen Mailer And Storage, Sterile |
| Product codes | FMH, KDT |
| Device classes | Class I |
| Medical specialties | Pathology |
| Brand names | NovoSort; Protex; ProteX Safe-Seal; ProteX Flight Lock |
| First new listing | 2026-06-03 |
| Latest new listing | 2026-06-03 |
| FDA registration number | 3018015381 |
| Registration expires | 2026-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- U.S. establishment.

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.