Home › Device types › LNQ
Intestinal Stimulator
FDA product code LNQ · Class f · Unknown
20
Registered devices
4,382
Adverse events
1
Recalls
0
510(k) clearances
Devices with this code
Enterra ReliaStim Unipolar Lead — Enterra Medical, Inc.N'VISION® — MEDTRONIC, INC.N'Vision — MEDTRONIC, INC.ENTERRA® II — MEDTRONIC, INC.N'VISION™ — MEDTRONIC, INC.ENTERRA® — MEDTRONIC, INC.ENTERRA® II — MEDTRONIC, INC.N'VISION™ — MEDTRONIC, INC.N'VISION™ — MEDTRONIC, INC.ENTERRA ™ — MEDTRONIC, INC.N'VISION™ — MEDTRONIC, INC.Enterra® II — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.ENTERRA ™ — MEDTRONIC, INC.ENTERRA® — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.N'VISION® — MEDTRONIC, INC.Enterra® II — MEDTRONIC, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2009-08-25 | Medtronic Neuromodulation | Medtronic is in the process of updating the Enterra Therapy labeling to include information regarding the risks of bowel obstruction and/or perforation. Medtro |
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