# Innopex Limited (foreign exporter, Toronto Ontario, CA): 89 new FDA device listings, incl. dressing, wound, occlusive

**Score:** 65/100

| Field | Value |
|---|---|
| Establishment | Innopex Limited |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Toronto Ontario, CA |
| New listings | 89 |
| Devices | Dressing, Wound, Occlusive; System, Transport, Aerobic; Syringe, Piston; Catheter, Urological; Syringe, Irrigating (Non Dental); Catheter, Irrigation; Catheter, Ureteral, Gastro-Urology; Tubes, Vials, Systems, Serum Separators, Blood Collection; Dressing, Wound, Drug; Container, Specimen, Sterile |
| Product codes | NAD, JTW, FMF, KOD, KYZ, GBX, EYB, JKA, FRO, FMH, KGZ, OEA, KNT, PIF, FPA |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | General, Plastic Surgery, Microbiology, General Hospital, Gastroenterology, Urology, Clinical Chemistry, Pathology, Anesthesiology, Physical Medicine, Neurology, Cardiovascular |
| Brand names | Syringe Piston; wound dressing; surgical cap; Blood collection tubes; Needle Injection Dispossable |
| First new listing | 2026-05-05 |
| Latest new listing | 2026-10-15 |
| FDA registration number | 3001124136 |
| Registration expires | 2027-12-31 |

## Why this score
- Class II or III devices: QMS and regulatory demands.
- Several new listings at once.
- 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.