# I-Tek Medical, Inc. (contract manufacturer, White Bear Lake, MN): 2 new FDA device listings, incl. cannula, surgical, general & plastic surgery

**Score:** 50/100

| Field | Value |
|---|---|
| Establishment | I-Tek Medical, Inc. |
| Role | Contract manufacturer |
| Establishment types | Manufacture Medical Device for Another Party (Contract Manufacturer); Complaint File Establishment per 21 CFR 820.198 |
| Location | White Bear Lake, MN, US |
| New listings | 2 |
| Devices | Cannula, Surgical, General & Plastic Surgery; Dropper, Ent |
| Product codes | GEA, KCM |
| Device classes | Class I |
| Medical specialties | General, Plastic Surgery, Ear, Nose, Throat |
| Brand names | 2-CAN |
| First new listing | 2026-05-19 |
| Latest new listing | 2026-09-21 |
| FDA registration number | 3008627763 |
| Registration expires | 2026-12-31 |

## Why this score
- Contract manufacturer or sterilizer adding work.
- 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.