FDA applicant
Technolab Industries (Canada), Ltd.
FDA records 1 decision for Technolab Industries (Canada), Ltd. (Montreal, Quebec, CA) in 1994: 1 510(k) clearance. All are in product code FLK (Thermometer, Clinical Mercury). 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 Technolab Industries (Canada), Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Technolab Industries (Canada), Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Technolab Industries (Canada), 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