FDA applicant

Spring Intl., Inc.

Schaumburg, IL1 decision1995–19950 recalls

FDA records 1 decision for Spring Intl., Inc. (Schaumburg, IL) in 1995: 1 510(k) clearance. All are in product code EFQ (Gauze/Sponge, Internal). No recall is linked to its devices.

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

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

FDA decisions per year

No FDA decision for Spring Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Spring Intl., 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 “Spring”

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

Spring Health Products, Inc. 1

Spring Intl., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Spring”