FDA applicant

Southland Instruments, Inc.

Minneapolis, MN2 decisions1984–19850 recalls

FDA records 2 decisions for Southland Instruments, Inc. (Minneapolis, MN) from 1984 to 1985: 2 510(k) clearances. All are in product code GAA (Needle, Aspiration And Injection, Disposable). 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, general and plastic surgery panel, where it files most

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

FDA decisions per year

No FDA decision for Southland Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Southland Instruments, 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 “Southland”

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

Southland Products Co., Ltd. 3 Southland, Ltd. 1

Southland Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Southland”