# EPIC MedTec OEM Catheter & Wire LLC (contract manufacturer, Plymouth, MN): 14 new FDA device listings, incl. introducer, catheter

**Score:** 90/100

| Field | Value |
|---|---|
| Establishment | EPIC MedTec OEM Catheter & Wire LLC |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer) |
| Location | Plymouth, MN, US |
| New listings | 14 |
| Devices | Introducer, Catheter; Transducer, Pressure, Catheter Tip; Catheter, Percutaneous; Port & Catheter, Implanted, Subcutaneous, Intravascular; Stent, Ureteral; Set, Administration, Intravascular; Accessories, Catheter, G-U |
| Product codes | DYB, DXO, DQY, LJT, FAD, FPA, KNY |
| Device classes | Class II |
| Medical specialties | Cardiovascular, General Hospital, Gastroenterology, Urology |
| First new listing | 2026-09-24 |
| Latest new listing | 2026-09-24 |
| FDA registration number | 3005232773 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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: 2026-11-04T21:52:36.524Z.
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.