FDA applicant

Mariner Biomedical, Inc.

Guilford, CT1 decision1996–19960 recalls

FDA records 1 decision for Mariner Biomedical, Inc. (Guilford, CT) in 1996: 1 510(k) clearance. All are in product code KMF (Bandage, Liquid). 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 hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Mariner Biomedical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Mariner Biomedical, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Mariner”

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

Mariner Endosurgery, Inc. 1

Mariner Biomedical, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Mariner”