Laborie Medical Technologies, Corp.
Laborie Medical Technologies, Corp. holds FDA 510(k) medical device clearances, first cleared 2008, most recent 2024, with 2 FDA device recalls on record.
Top product codes for Laborie Medical Technologies, Corp.
FDA recalls by Laborie Medical Technologies, Corp.
- Z-2669-2026 — Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM H2O, 24p, Compact Pole system (G3-7), Solar GI HRM H2O, 24p, Trolley system (G3-8), Solar GI HRM H2O, 36p, Trolley system (G3-12), Solar GI HRAM H2O, 24p, Trolley system (G3-14);
- Z-2076-2019 — U3-3 Solar Blue, Laptop integrated power supply used with the Solar Blue Urodynamics for assessing lower urinary tract dysfunctions
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Laborie Medical Technologies, Corp.
Data sourced from openFDA. This site is unofficial and independent of the FDA.