FDA applicant

Vascor, Inc.

Walker, MI2 decisions1981–19810 recalls

FDA records 2 decisions for Vascor, Inc. (Walker, MI) in 1981: 2 510(k) clearances. All are in product code DTJ (Holder, Heart-Valve, Prosthesis). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Vascor, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Vascor”

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

Vascor Medical Corp. 3

Vascor, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Vascor”