Data / Medical devices / Canada / AG Marketing & Development Group Inc Dba Agmd Group
AG Marketing & Development Group Inc Dba Agmd Group: FDA-registered device maker in Brampton Ontario, Canada, 33 510(k) clearances and 1 PMA approval
AG Marketing & Development Group Inc Dba Agmd Group is registered with the FDA (registration 3016844398) in Brampton Ontario, Canada. It lists 28 device types. The FDA files 33 510(k) clearances and 1 PMA approval under its listings, the newest dated April 15, 2026. Registered through 2027. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3016844398
- Address
- 2600 N Park Dr, Brampton Ontario, Canada, L6S 6E2
- Owner or operator
- Ag Marketing & Development Group Inc Dba Agmd Group (10089735)
- Roles
- Exporter to the US, Foreign private label distributor, Repackager or relabeler
- First device listed
- January 3, 2024
- Registered through
- 2027
- Brand names listed
- AR LOOP PROCEDURE MASK / TIE-ON SURGICAL MASK / EAR LOOP PROCEDURE MASK WITH SHIELD, CISION Disposable Surgical Scalpel, Intco Basic Diamond Textured Nitrile Gloves 8 Mil Black, Medline Disposable Surgical Drapes and Gowns, Medline Surgical Mask, Primagard Isolation Gown, SYNTHETIC POWDER-FREE NITRILE PATIENT EXAMINATION GLOVES
Devices it lists
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| April 15, 2026 | K260128 | BD Preset and BD A-Line Arterial Blood Collection Syringes | JKA | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| January 31, 2025 | K243441 | Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid (Light blue, Dark blue) | LZA | Substantially Equivalent | Basic Medical Technology, Inc. | accessdata.fda.gov |
| July 21, 2023 | K221327 | BD Alaris Pump Infusion Sets | FPA | Substantially Equivalent | Care Fusion | accessdata.fda.gov |
| October 11, 2022 | K222744 | Sol-M Luer Lock Syringe | FMF | Substantially Equivalent | Sol-Millennium Medical, Inc. | accessdata.fda.gov |
| June 16, 2022 | K221226 | 1st Glove Blue Nitrile Examination Gloves Powder Free | LZA | Substantially Equivalent | Koove Iot Pvt. , Ltd. | accessdata.fda.gov |
| March 30, 2021 | K202708 | Surgical Face Masks | FXX | Substantially Equivalent | Intco Medical(Hk) Co., Ltd. | accessdata.fda.gov |
| August 4, 2020 | K193666 | Powder-Free Blue Nitrile Examination Gloves (Tested for use with Chemotherapy and Fentanyl) Regular Cuff; Powder-Free Blue Nitrile Examination Gloves (Tested for use with Chemotherapy Drugs and Fentanyl) - Extended Cuff | LZA | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| January 10, 2020 | K192315 | Medline Green Ambidextrous Power-Free Nitrile Examination Gloves with Colloidal Oatmeal USP (Tested for Use with Chemotherapy Drugs) | LZA | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| September 17, 2019 | K190308 | Medicom SafeMask Sofskin Pediatric Procedure Earloop Face Masks (ASTM Level 1), Medicom SafeMask Sofskin Pediatric Procedure Earloop Face Masks, Medicom SafeMask Premier Pediatric Procedure Earloop Face Masks (ASTM Level 1), Medicom SafeMask Premier Pediatric Procedure Earloop Face Masks (ASTM Level 1) | OXZ | Substantially Equivalent | Amd Medicom, Inc. | accessdata.fda.gov |
| June 20, 2019 | K190095 | Powder-Free Clear Vinyl Patient Examination Gloves | LYZ | Substantially Equivalent | Anhui Intco Medical Products Co., Ltd. | accessdata.fda.gov |
| December 3, 2018 | K182146 | Sol-M Blood Collection Needles, Sol-Care Safety Blood Collection Needles, Sol-Care Safety Blood Collection Needle with Holders, Sol-M Blood Collection Set | FMI | Substantially Equivalent | Sol-Millennium Medical, Inc. | accessdata.fda.gov |
| April 10, 2018 | K180233 | Eviva Stereotactic Guided Breast Biopsy System | KNW | Substantially Equivalent | Hologic, Inc. | accessdata.fda.gov |
| November 4, 2016 | K160361 | PRIMAGARD Isolation Gown (AAMI PB70 Level 3) | FYC | Substantially Equivalent | Primed Medical Products, Inc. | accessdata.fda.gov |
| June 17, 2016 | K153537 | Sol-M Insulin Syringe, Sol-M TB Syringe | FMF | Substantially Equivalent | Sol-Millennium Medical, Inc. | accessdata.fda.gov |
| June 18, 2015 | K150340 | POWDER FREE Nitrile GLOVES (White), POWDER FREE Nitrile GLOVES (Cobalt Blue), POWDER FREE Nitrile GLOVES (Black), POWDER FREE Nitrile GLOVES (Ice Blue) | LZA | Substantially Equivalent | Hebei Hongsen Plastics Technology Co, Ltd. | accessdata.fda.gov |
| March 14, 2014 | K131796 | MANUKA FILL WOUND DRESSING | FRO | Substantially Equivalent | Links Medical Products, Inc. | accessdata.fda.gov |
| February 24, 2012 | K112777 | SOL-M EXCHANGEABLE NEEDLES | FMI | Substantially Equivalent | Sol-Milennium Medical, Inc. | accessdata.fda.gov |
| May 13, 2011 | K110771 | BD SINGLE USE, HYPODERMIC SYRINGE | FMF | Substantially Equivalent | Becton, Dickinson and Company | accessdata.fda.gov |
| April 15, 2011 | K110921 | NITRILE POWDER-FREE EXAMINATION GLOVES TESTED FOR USE WITH CHEMOTHERAPY DRUGS | LZA | Substantially Equivalent | Cardinal Health, Inc. | accessdata.fda.gov |
| April 3, 2009 | K090352 | TAPERGUARD ENDOTRACHEAL TUBES, TAPERGUARD EVAC ENDOTRACHEAL TUBES | BTR | Substantially Equivalent | Covidien | accessdata.fda.gov |
| April 24, 2006 | K060865 | BAIR PAWS TEMPERATURE MANAGEMENT SYSTEM MODEL 850 | DWJ | Substantially Equivalent | Arizant Healthcare, Inc. | accessdata.fda.gov |
| September 20, 2005 | K051291 | NON-STERILE SURGICAL MASK | FXX | Substantially Equivalent | A.R. Medicom, Inc. | accessdata.fda.gov |
| August 3, 2005 | K051378 | POWDER-FREE BLUE NITRILE EXAMINATION GLOVES (TESTED FOR USE WITH CHEMOTHERAPY DRUGS) | LZA | Substantially Equivalent | Medline | accessdata.fda.gov |
| June 10, 2003 | K023755 | WINNER EAR LOOP PROCEDURE MASK, TIE-ON SURGICAL MASK & EAR LOOP PROCEDURE MASK WITH SHIELD | FXX | Substantially Equivalent | Winner Industries (Shenzhen) Co., Ltd. | accessdata.fda.gov |
| July 19, 2002 | K021475 | BD SINGLE LUMEN NEEDLE, SYRINGE AND BLOOD COLLECTION SET | FMI | Substantially Equivalent | Bd | accessdata.fda.gov |
| August 30, 1999 | K990310 | CHARTER MEDICAL, LTD MP 450 (40 MICRON FILTER) | CAK | Substantially Equivalent | Charter Medical, Ltd. | accessdata.fda.gov |
| August 23, 1999 | K991559 | MEDLINE PROHIBIT SERIES SURGICAL MASK WITH FLUID SHIELD | FXX | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| April 30, 1998 | K973741 | BAIR HUGGER BLOOD/FLUID WARMER | BSB | Substantially Equivalent | Augustine Medical, Inc. | accessdata.fda.gov |
| February 25, 1997 | K964142 | MEDLINE DISPOSABLE SURGICAL DRAPES AND GOWNS | KKX | Substantially Equivalent | Medline Industries, Inc. | accessdata.fda.gov |
| October 7, 1995 | K951254 | SAFETYGLIDE NEEDLE | FMI | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| July 14, 1995 | K942988 | FILTERED EXTENSION SETS | FPA | Substantially Equivalent | B. Braun of America, Inc. | accessdata.fda.gov |
| May 26, 1994 | K941562 | 1ML LUER-LOK SYRINGE | FMF | Substantially Equivalent | Bd Becton Dickinson Vacutainer Systems Preanalytic | accessdata.fda.gov |
| November 5, 1979 | K791871 | NEUROLOGICAL SPONGES (PATTIES) | EFQ | Substantially Equivalent | Carwild Corp. | accessdata.fda.gov |
PMA approvals
Premarket approvals this establishment lists, with the supplements the FDA has decided since.
| Approved | PMA number | Device | Product code | Supplements | Latest decision | Source |
|---|---|---|---|---|---|---|
| September 30, 1999 | P990004 | SURGIFOAM ABSORBABLE GELATIN SPONGE, USP | LMF | 79 | September 18, 2026 | accessdata.fda.gov |
Compare with other makers
- All makers of Vinyl Patient Examination Glove
- All makers of Polymer Patient Examination Glove
- All makers of Tubes, Vials, Systems, Serum Separators, Blood Collection
- All makers of Gauze/Sponge, Internal
- All makers of Mask, Surgical
- All makers of Latex Patient Examination Glove
Updated September 18, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.