# MEDLINE INDUSTRIES, LP - Northfield (specification developer, Northfield, IL): 144 new FDA device listings, incl. wrap, sterilization

**Score:** 95/100

| Field | Value |
|---|---|
| Establishment | MEDLINE INDUSTRIES, LP - Northfield |
| Owner / operator | Medline Industries, LP |
| 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 | Northfield, IL, US |
| New listings | 144 |
| Devices | Wrap, Sterilization; Visual, Pregnancy Hcg, Prescription Use; Drink, Glucose Tolerance; Suture, Nonabsorbable, Synthetic, Polyethylene; Pediatric Position Holder; Helicobacter Pylori; Set, Administration, Intravascular; Regulator, Vacuum; System, Blood Collection, Vacuum-Assisted, Manual; Chair And Table, Medical |
| Product codes | FRG, JHI, MRV, GAT, PRN, LYR, FPA, KDP, KST, KMN, ILC, KIA, MQV, IQF, IPG |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General Hospital, Clinical Chemistry, General, Plastic Surgery, Microbiology, Hematology, Physical Medicine, Orthopedic, Obstetrics/Gynecology, Dental, Gastroenterology, Urology, Anesthesiology, Pathology, Cardiovascular, Neurology, Immunology, Ophthalmic, Clinical Toxicology |
| Brand names | Medline; TYVEK; Medline UNITE HS Fiber; ORNEX; MedStop; Medline Blood Collection Tube Holder; Medline Tongue Blade; CURAD |
| First new listing | 2026-05-01 |
| Latest new listing | 2026-10-08 |
| FDA registration number | 1417592 |
| 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.
- 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: 2026-10-28T20:51:27.468Z.
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.