Data / Medical devices / United States / Vineland Syrup Inc.
Vineland Syrup Inc.: FDA-registered device maker in Vineland, NJ, United States, 1 510(k) clearance
Vineland Syrup Inc. is registered with the FDA (registration 2226984) in Vineland, NJ, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated June 21, 2012. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 2226984
- Address
- 723 S.E. BLVD., Vineland, NJ, United States, 08360
- Owner or operator
- VINELAND SYRUP INC. (9058089)
- Roles
- Manufacturer
- First device listed
- June 25, 2012
- Registered through
- 2026
- Brand names listed
- EasyDex
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Drink, Glucose Tolerance | MRV | 2 | Manufacturer | accessdata.fda.gov |
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 |
|---|---|---|---|---|---|---|
| June 21, 2012 | K120247 | EASYDEX | MRV | Substantially Equivalent | Vineland Syrup, Inc. | accessdata.fda.gov |
Compare with other makers
Updated June 21, 2012. 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.