FDA applicant

Vineland Syrup, Inc.

Sewell, NJ1 decision2012–20120 recalls

FDA records 1 decision for Vineland Syrup, Inc. (Sewell, NJ) in 2012: 1 510(k) clearance. All are in product code MRV (Drink, Glucose Tolerance). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Vineland Syrup, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2012

2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Vineland Syrup, Inc. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Vineland Syrup, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Vineland”

FDA records each applicant name separately; these may or may not be the same firm.

Vineland Medical Products, Inc. 1

Vineland Syrup, Inc.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Vineland”