ClearanceBrief
Company · US

Longeviti Neuro Solutions, LLC

FDA 510(k) clearances and medical device recalls filed under this name, 2018 to 2026. Name variants (Inc, Corp, punctuation) are merged.

9510(k) clearances (1 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
GXNPlate, Cranioplasty, Preformed, Non-Alterable8
KKYMaterial, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 25, 2026K260709ClearFit Ti Ring 14mm (171750);ClearFit Ti Ring 14mm with Slot (171751);ClearFit Ti Ring 20mm (171752);ClearFit Ti Ring
Longeviti Neuro Solutions
GXN
Nov 9, 2023K231920Longeviti ClearFit OTS Cranial Implant
Longeviti Neuro Solutions, LLC
GXN
Sep 8, 2021K212058Longeviti ClearFit™ OTS Cranial Implants
Longeviti Neuro Solutions, LLC
GXN
Jul 15, 2021K211514Longeviti PorousFit implant
Longeviti Neuro Solutions, LLC
KKY
Mar 31, 2021K210616Longeviti PMMA Static Cranial Implant
Longeviti Neuro Solutions, LLC
GXN
Dec 16, 2020K203349Longeviti ClearFit Cranial Implant
Longeviti Neuro Solutions, LLC
GXN
Oct 30, 2020K202901Longeviti ClearFit Cranial Implant
Longeviti Neuro Solutions, LLC
GXN
Jan 9, 2020K191210Longeviti ClearFit Cranial Implant
Longeviti Neuro Solutions, LLC
GXN
Mar 23, 2018K170410Longeviti PMMA Static Cranial Implant
Longeviti Neuro Solutions, LLC
GXN

Latest recalls

DateFirm and productCodeLinked 510(k)
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