FDA applicant
Anago, Inc.
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
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.
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.
See the 510(k) Report