FDA applicant
Travis Industries, Inc.
FDA records 3 decisions for Travis Industries, Inc. (Coos Bay, OR) in 1990: 3 510(k) clearances. All are in product code KPN (Alarm, Conditioned Response Enuresis). 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 Travis Industries, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Travis Industries, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Travis Industries, 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