Longeviti Neuro Solutions

FDA Regulatory Profile

Longeviti Neuro Solutions appears in FDA public data with 0 recalls, 9 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 25, 2026.

Summary

Total Recalls
0
510(k) Clearances
9
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K260709ClearFit Ti Ring 14mm (171750);ClearFit Ti Ring 14mm with Slot (171751);ClearFit Ti Ring 20mm (17175June 25, 2026
K231920Longeviti ClearFit OTS Cranial ImplantNovember 9, 2023
K212058Longeviti ClearFit™ OTS Cranial ImplantsSeptember 8, 2021
K211514Longeviti PorousFit implantJuly 15, 2021
K210616Longeviti PMMA Static Cranial ImplantMarch 31, 2021
K203349Longeviti ClearFit Cranial ImplantDecember 16, 2020
K202901Longeviti ClearFit Cranial ImplantOctober 30, 2020
K191210Longeviti ClearFit Cranial ImplantJanuary 9, 2020
K170410Longeviti PMMA Static Cranial ImplantMarch 23, 2018