# Patterson Dental Canada Inc. (repackager or relabeler, Montreal Quebec, CA): 4 new FDA device listings, incl. device, caries detection

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | Patterson Dental Canada Inc. |
| Owner / operator | Patterson Companies, Inc. |
| Role | Repackager or relabeler |
| Establishment types | Foreign Private Label Distributor; Repack or Relabel Medical Device |
| Location | Montreal Quebec, CA |
| New listings | 4 |
| Devices | Device, Caries Detection; Handpiece, Air-Powered, Dental; Cord, Retraction; Resin, Root Canal Filling |
| Product codes | LFC, EFB, MVL, KIF |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Dental |
| Brand names | Caries Indicator; Patterson K-Spray; Hemo Gel 20%/ 25% / Ferric Sulfate 15.5%; Bioactive Endosealer |
| First new listing | 2026-06-01 |
| Latest new listing | 2026-08-04 |
| FDA registration number | 3000219976 |
| Registration expires | 2026-12-31 |

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

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.