510(k) Report

FDA applicant

Anago, Inc.

Fort Worth, TX44 decisions1979–19930 recalls

FDA records 44 decisions for Anago, Inc. (Fort Worth, TX) from 1979 to 1993: 44 510(k) clearances. Most are in product codes FXX (Mask, Surgical) and MMK (Container, Sharps). 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 Anago, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Anago, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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