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US
Last updated September 17, 2026
What NALU MEDICAL makes
NALU MEDICAL makes implantable analgesic electrical stimulation systems for spinal cord and peripheral nerve pain management, including pulse generators, leads with wired and wireless connections, and related components such as personal device holders and trial percutaneous pulse generators. They also produce non-medicated, single-use neurosurgical procedure kits.
Their devices are classified as Class II medical devices and are listed in the FDA's Unique Device Identification (fda_udi) registry. The company is based in the United States.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What does Nalu Medical make?
Nalu Medical makes implantable analgesic electrical stimulation systems for spinal cord and peripheral nerve pain management, including pulse generators, leads with wired and wireless connections, personal device holders, trial percutaneous pulse generators, and non-medicated, single-use neurosurgical procedure kits.
Where is Nalu Medical based?
Nalu Medical is based in the United States, as stated in the provided device data under the COUNTRY field.
Which registries list Nalu Medical's devices?
Nalu Medical's devices are listed in the FDA's Unique Device Identification (fda_udi) registry, as specified in the LISTED IN field of the device data.
How are Nalu Medical's devices classified?
Nalu Medical's devices are classified as Class II medical devices, according to the DEVICE CLASSES field in the provided data.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
- 2320 Faraday Ave., Carlsbad, CA, 92008
- Website
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- —
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- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3015425075
- DUNS Number
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Catalogue (297)
Page 1 of 6| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Nalu Medical, Inc. | 72003 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72006-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12002-030-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72001 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23007 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23003-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71006-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23003-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12001-040 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23007-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71007-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12003-035-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-065 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72006 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72007 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23007 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 53002-001 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23006-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-025 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72003-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-030-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23004-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72005-US | FDA UDI | Class II | Unknown |
| Nalu Medical, Inc. | 71010-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23013-050-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74007-002-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23003-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72012-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-065-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74007-002-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-045-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74008-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71019-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 72002 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74001-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-030-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71005-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 34007-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71004-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23012-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23002-045 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 71007-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 23001-060-US | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12001-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 12007-060 | FDA UDI | Class II | Active |
| Nalu Medical, Inc. | 74002-US | FDA UDI | Class II | Active |
Related Companies
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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.
There is 1 recall record for NALU MEDICAL, initiated on 2024-06-03, with statuses recorded as open and classified. The reason given is a manufacturing non-conformance in Neurostimulation Systems that may reduce the efficiency of radiofrequency signals between the Implantable Pulse Generator and the Therapy Disc, potentially causing the IPG to be non-functional and the device to no longer inhibit.
AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.
| 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. |