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US
Last updated September 17, 2026
Information
- Country
- US
- Address
- 2320 Faraday Ave., Carlsbad, CA, 92008
- Website
- —
- —
- —
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3015425075
- DUNS Number
- —
Catalogue (297)
Page 2 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nalu Medical, Inc. | 23012-065-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23006-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72004-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-025-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23013-050-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23005-003 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12006-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-065-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72007-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23013-050 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72005 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12003-035 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74007-002-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12001-040-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-030 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12005-040-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74007-003-US | FDA UDI | Class II | Active |
| Nalu Medical | 71003 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 34004-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 34011-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72006 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12007-040-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72013-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 34009-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72005-US | FDA UDI | Class II | Unknown |
| Nalu Medical, Inc. | 12007-040 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23003-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74002 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-045 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 13001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23003-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12005-025 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74002-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23004 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23006 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71005-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12002-030-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23006 | FDA UDI | Class II | Active |
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FDA Recalls (1)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| Jun 3, 2024 | Z-2257-2024 | — | open, classified | Neurostimulation Systems have a manufacturing non-conformance that may reduce the efficiency of the radiofrequency signals between the Implantable Pulse Generator (IPG) and the Therapy Disc, causing the IPG to be non-functional, which causes the device to be non-functional so it will no longer inhibit the transmission of pain signals to the brain. |