FDA applicant

Vector Corporation, LLC

New York, NY2 decisions1996–20150 recalls

FDA records 2 decisions for Vector Corporation, LLC (New York, NY) from 1996 to 2015: 2 510(k) clearances. Most are in product codes LIT (Catheter, Angioplasty, Peripheral, Transluminal) and BYG (Mask, Oxygen). Its devices cite 1 predicate, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Vector, Inc.”.

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

FIG. A — Illustration, cardiovascular panel, where it files most

How often FDA has decided Vector Corporation, LLC’s devices, and how often a recall has named them.

FDA decisions per year

1in 2015

2007high 1 (2015) · low 0 (2007)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vector Corporation, LLC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Vector”

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

Vector Medical, Inc. 2 Vector Mobility, Inc. 2 Vector Research & Development 1

Vector Corporation, LLC

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Vector”