FDA applicant

Gresco International, Inc.

San Antonio, TX1 decision1988–19880 recalls

FDA records 1 decision for Gresco International, Inc. (San Antonio, TX) in 1988: 1 510(k) clearance. All are in product code DQR (Cannula, Catheter). 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 Gresco International, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gresco International, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Gresco International, 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 “Gresco”

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

Gresco Products, Inc. 7

Gresco International, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Gresco”