# K143711: Reaxon Plus

- Pathway: 510(k) (Traditional)
- Applicant: Medovent GmbH
- Decided: Dec 2, 2015 after 338 days
- Product code: JXI (Cuff, Nerve)
- Device class: 2
- Regulation: 21 CFR 882.5275
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K011168 (2001). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K011168: Neurogen Nerve Guide, Integra Lifesciences Corp. (2001) Summary page 5.

## Most influential descendants
- K190246: NeuroShield (2019), 0 descendants of its own

## Indications for use
Reaxon® Plus is indicated for repair of peripheral nerve discontinuities up to 10 mm and where gap closure can be achieved by flexion of the extremity.

Source page: https://510kreport.com/device/K143711
Methodology: https://510kreport.com/methodology