# AG Marketing & Development Group Inc Dba Agmd Group (foreign exporter, Brampton Ontario, CA): 20 new FDA device listings, incl. tubes, vials, systems, serum separators, blood collection

**Score:** 55/100

| Field | Value |
|---|---|
| Establishment | AG Marketing & Development Group Inc Dba Agmd Group |
| Owner / operator | Ag Marketing & Development Group Inc Dba Agmd Group |
| Role | Foreign exporter |
| Establishment types | Export Device to the United States But Perform No Other Operation on Device |
| Location | Brampton Ontario, CA |
| New listings | 20 |
| Devices | Tubes, Vials, Systems, Serum Separators, Blood Collection; Needle, Hypodermic, Single Lumen; Syringe, Piston; Polymer Patient Examination Glove; Mask, Surgical; Warmer, Blood, Non-Electromagnetic Radiation; Vinyl Patient Examination Glove; Needle, Aspiration And Injection, Disposable; Set, Administration, Intravascular; Pediatric/Child Facemask |
| Product codes | JKA, FMI, FMF, LZA, FXX, BSB, LYZ, GAA, FPA, OXZ, OPJ, LZC, QDO, EFQ |
| Device classes | Class I, Class II, Unclassified |
| Medical specialties | Clinical Chemistry, General Hospital, General, Plastic Surgery, Hematology |
| First new listing | 2026-05-01 |
| Latest new listing | 2026-08-25 |
| FDA registration number | 3016844398 |
| 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.