FDA Device Intelligence
HomeDevice types › LEI

Implant, Anti-Gastroesophageal Reflux

FDA product code LEI · Class 3 · Unknown

19
Registered devices
2,236
Adverse events
5
Recalls
0
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2018-04-20Torax Medical, Inc.Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or
2018-04-20Torax Medical, Inc.Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or
2018-04-20Torax Medical, Inc.Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or
2018-04-20Torax Medical, Inc.Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or
2018-04-20Torax Medical, Inc.Possible out of specification condition which may allow a bead component to separate from an adjacent wire link. This condition may result in a discontinuous or

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.