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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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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: —

Catalogue (145)

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Device	Model / Reference	Registries	Class	Status
Spinal Jaxx Interbody Fusion Device	100001-561	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-555	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-313	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-571	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-523	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-576	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-306	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-547	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-505	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-636	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-531	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-503	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-640	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-645	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-526	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-345	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-565	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-311	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-574	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-539	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-543	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-567	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-549	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-558	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-554	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-572	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-628	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-575	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-643	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-528	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-540	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-630	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-381	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-304	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-546	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-577	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-563	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-508	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-309	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-534	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-541	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-310	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-566	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-524	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	K152501	FDA 510(k)	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.

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.