# Bard Access Systems, Inc. (other, Salt Lake City, UT): 14 new FDA device listings, incl. catheter, umbilical artery

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Bard Access Systems, Inc. |
| Owner / operator | C. R. Bard, Inc. |
| Role | Other |
| Establishment types | Complaint File Establishment per 21 CFR 820.198 |
| Location | Salt Lake City, UT, US |
| New listings | 14 |
| Devices | Catheter, Umbilical Artery; Tourniquet, Nonpneumatic; Introducer, Catheter; Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days; Tubes, Gastrointestinal (And Accessories); Catheter, Straight; Drape, Surgical, Exempt; Kit, Surgical Instrument, Disposable; Cutter, Surgical |
| Product codes | FOS, GAX, DYB, LJS, KNT, EZD, PUI, KDD, FZT |
| Device classes | Class I, Class II |
| Medical specialties | General Hospital, General, Plastic Surgery, Cardiovascular, Gastroenterology, Urology |
| Brand names | Footprint Medical Dual-Lumen Umbilical Catheter; Tourniquet, non-pneumatic; Footprint Medical PICC Introducer; Footprint Medical Polyurethane PICC; Footprint Medical Polyurethane Feeding Tube; Footprint Medical Urinary Drainage Catheter; Drape, surgical; Footprint Medical Silicone PICC |
| First new listing | 2026-08-05 |
| Latest new listing | 2026-08-14 |
| FDA registration number | 3006260740 |
| Registration expires | 2026-12-31 |

## Why this score
- 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: 2026-10-28T20:51:27.468Z.
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.