FDA applicant

Santerra Medical Technology, Inc.

Lake Elmo, MN1 decision1999–19990 recalls

FDA records 1 decision for Santerra Medical Technology, Inc. (Lake Elmo, MN) in 1999: 1 510(k) clearance. All are in product code FTL (Mesh, Surgical, Polymeric). 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 Santerra Medical Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Santerra Medical Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Santerra Medical Technology, Inc.

Which product codes does it file in?

What has FDA decided for it lately?