FDA applicant
Terayco Intl., Ltd.
FDA records 3 decisions for Terayco Intl., Ltd. (Mchenry, IL) from 1983 to 1985: 3 510(k) clearances. Most are in product codes FLL (Continuous Measurement Thermometer) and HGY (Pump, Breast, Non-Powered). 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 Terayco Intl., Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Terayco Intl., Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Terayco Intl., Ltd.’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