# Medron, LLC (contract manufacturer, Salt Lake City, UT): 2 new FDA device listings, incl. midline catheter

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Medron, LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Salt Lake City, UT, US |
| New listings | 2 |
| Devices | Midline Catheter; Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days |
| Product codes | PND, LJS |
| Device classes | Class II |
| Medical specialties | General Hospital |
| Brand names | BioFlo Hybrid PICC with Endexo and PASV Valve Technology; BioFlo Midline Catheter; Xcela Hybrid PICC with PASV Valve Technology; Xcela Power Injectable PICC; BioFlo PICC with Endexo and PASV Valve Technology; BioFlo PICC with Endexo Technology; Xcela PICC with PASV Valve Technology |
| First new listing | 2026-09-14 |
| Latest new listing | 2026-09-14 |
| FDA registration number | 1722746 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- 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.