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Neuropro Spinaljaxx, Inc.

Last updated May 23, 2026

What Neuropro Spinaljaxx, Inc. makes

Neuropro Spinaljaxx, Inc. makes spinal interbody fusion cages, both polymeric and metallic, as well as kits and instruments for orthopaedic procedures, including bone graft delivery kits, surgical instrument/implant depth limiters, and orthopaedic inorganic implant inserters/extractors.

The company's portfolio is classified as Class II devices and is listed in the FDA 510(k) and FDA UDI registries, with the company based in the US.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What type of devices does Neuropro Spinaljaxx, Inc. manufacture?

Neuropro Spinaljaxx, Inc. makes spinal interbody fusion cages and kits for orthopaedic procedures, including bone graft delivery kits and surgical instruments, as these are listed in their device categories.

Where is Neuropro Spinaljaxx, Inc. based?

The company is based in the US, as indicated in the provided data.

Which registries list Neuropro Spinaljaxx, Inc.'s devices?

The company's devices are listed in the FDA 510(k) and FDA UDI registries, which track medical devices.

How are Neuropro Spinaljaxx, Inc.'s devices classified?

The company's devices are classified as Class II, which is a specific category of medical devices.

AI-generated from registry data and not verified by a human reviewer.

Information

Country: US
Address: —
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EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (145)

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Device	Model / Reference	Registries	Class	Status
Spinal Jaxx Interbody Fusion Device	100001-515	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-532	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-559	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-312	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-509	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-624	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-550	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-315	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-618	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-506	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-639	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-301	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-507	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-325	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-501	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-538	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-620	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-634	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-504	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-633	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-518	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-365	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-308	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-502	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-385	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-631	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-646	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-632	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-517	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-637	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-382	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-512	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-579	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-553	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-556	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-644	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-581	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-641	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-520	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-615	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-627	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-626	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-580	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-629	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-303	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-551	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-562	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-511	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-305	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-390	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 Neuropro Spinaljaxx, Inc., which was initiated on 2018-01-18. The status of this recall is recorded as terminated. The reason given for the recall is that the implant size is incorrectly etched on the implant, while the size listed on the box is correct.

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
Jan 18, 2018	Z-1350-2018	—	terminated	The implant size is incorrectly etched on the implant. The size listed on the box is correct.