# MEDLINE INDUSTRIES, LP (Northpoint Services) (contract sterilizer, Waukegan, IL): 46 new FDA device listings, incl. tourniquet, pneumatic

**Score:** 90/100

| Field | Value |
|---|---|
| Establishment | MEDLINE INDUSTRIES, LP (Northpoint Services) |
| Owner / operator | Medline Industries, LP |
| Role | Contract sterilizer |
| Establishment types | Sterilize Medical Device for Another Party (Contract Sterilizer) |
| Location | Waukegan, IL, US |
| New listings | 46 |
| Devices | Tourniquet, Pneumatic; Catheter, Recording, Electrode, Reprocessed; Catheter, Intracardiac Mapping, High-Density, Reprocessed; Septostomy Catheter, Reprocessed; Reprocessed Intravascular Ultrasound Catheter; Set, Administration, Intravascular; Tubes, Gastrointestinal (And Accessories); Syringe, Piston; Reprocessed Catheter Introducer; Trocar, Reprocessed |
| Product codes | KCY, NLH, NLG, QLZ, OWQ, FPA, KNT, FMF, PNE, NMK, LXC, PNR, FZP, DSS |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General, Plastic Surgery, Cardiovascular, General Hospital, Gastroenterology, Urology |
| Brand names | ExpressAire Tourniquet Cuff; Color Cuff Cylindrical Tourniquet; Color Cuff Disposable Tourniquet; Tourniquet Cuff; EP XT Steerable; Decanav; IntellaMap Orion High; Webster Duo-Decapolar |
| First new listing | 2026-06-04 |
| Latest new listing | 2026-10-21 |
| FDA registration number | 1422634 |
| Registration expires | 2027-12-31 |

## 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.