FDA applicant
Allertech, Inc.
FDA records 1 decision for Allertech, Inc. (Littleton, CO) in 1988: 1 510(k) clearance. All are in product code LDH (Unnamed device). 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 Allertech, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Allertech, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Allertech, 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