# Teleflex Medical LLC (specification developer, Morrisville, NC): 4 new FDA device listings, incl. suture, nonabsorbable, synthetic, polyethylene

**Score:** 85/100

| Field | Value |
|---|---|
| Establishment | Teleflex Medical LLC |
| Owner / operator | Teleflex |
| Role | Specification developer (outsources manufacturing) |
| Establishment types | Complaint File Establishment per 21 CFR 820.198; Develop Specifications But Do Not Manufacture At This Facility |
| Location | Morrisville, NC, US |
| New listings | 4 |
| Devices | Suture, Nonabsorbable, Synthetic, Polyethylene; Catheter, Percutaneous; Suture, Surgical, Absorbable, Polydioxanone; Instrument, Biopsy |
| Product codes | GAT, DQY, NEW, KNW |
| Device classes | Class II |
| Medical specialties | General, Plastic Surgery, Cardiovascular, Gastroenterology, Urology |
| Brand names | Turnpike catheter, Turnpike Spiral catheter, Turnpike LP catheter, Turnpike Gold catheter, GuideLiner V3, Trapliner cath; OnControl Bone Access System |
| First new listing | 2026-06-26 |
| Latest new listing | 2026-07-31 |
| FDA registration number | 3011137372 |
| Registration expires | 2027-12-31 |

## Why this score
- Brings its own devices to market: buys manufacturing, sterilization and QMS help.
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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: 2026-11-04T21:52:36.524Z.
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.