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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)

Page 1 of 3

Device	Model / Reference	Registries	Class	Status
Spinal Jaxx Interbody Fusion Device	100001-578	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-522	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-513	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-622	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-545	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-300	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-557	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-552	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-529	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-307	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-564	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-544	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-514	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-573	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-330	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-360	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-525	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-510	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-642	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-635	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-302	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-521	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-314	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-548	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-335	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-384	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-619	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-568	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-383	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-536	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-569	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-616	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-638	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-625	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-340	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-535	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-623	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-530	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-527	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-560	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-516	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-570	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-621	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-350	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-542	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-355	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-519	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-537	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-617	FDA UDI	Class II	Active
Spinal Jaxx Interbody Fusion Device	100001-370	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.