FDA applicant

Fossa Industries, Inc.

Boston, MA2 decisions2002–20020 recalls

FDA records 2 decisions for Fossa Industries, Inc. (Boston, MA) in 2002: 2 510(k) clearances. All are in product code FAD (Stent, Ureteral). 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, gastroenterology and urology panel, where it files most

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

FDA decisions per year

No FDA decision for Fossa Industries, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fossa Industries, 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 “Fossa”

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

Fossa Medical, Inc. 3

Fossa Industries, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Fossa”