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Xtant Medical Holdings, Inc.

Last updated September 17, 2026

What Xtant Medical Holdings, Inc. makes

Xtant Medical Holdings, Inc. manufactures spinal devices including non-bioabsorbable spinal bone screws, polymeric and metallic spinal interbody fusion cages, non-bioabsorbable spinal fixation plates, bone-screw internal spinal fixation systems, bone taps, and interspinous spinal fixation implants. Specific products include the Streamline OCT, Cortera, Xspan Laminoplasty Fixation System, InTice™ -C Porous Ti Cervical Interbody System, Aranax Anterior Cervical Plating System, Calix Spinal Implant System, Fortex Pedicle Screw System, Cortera Spinal Fixation System, and Zyfix Spinal Facet Screw System.

The company's portfolio is regulated with devices classified as Class I, Class II, and U, and is listed in the FDA UDI registry. Xtant Medical Holdings, Inc. is 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 does Xtant Medical Holdings, Inc. manufacture?

Where is Xtant Medical Holdings, Inc. based?

Xtant Medical Holdings, Inc. is based in the US, as indicated in the device data provided.

Which registries list Xtant Medical's devices?

Xtant Medical's devices are listed in the FDA UDI registry, as specified in the device data.

How are Xtant Medical's devices classified?

Xtant Medical's devices are classified as Class I, Class II, and U, according to the regulatory classifications provided in the device data.

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

Information

Country: US
Address: 664 Cruiser Lane, Belgrade, MT, 59714
Website: —
LinkedIn: —
Facebook: —
Email: —
Phone: —
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3005031160
DUNS Number: —

Catalogue (9214)

Page 34 of 185

Device	Model / Reference	Registries	Class	Status
Fortex Pedicle Screw System	X022-0190	FDA UDI	Class II	Active
Cortera	150104-00090	FDA UDI	Class II	Active
Calix Spinal Implant System	X034-2789	FDA UDI	Class I	Active
Cortera Spinal Fixation System	150102-25060	FDA UDI	Class II	Active
Cortera	1505-000510	FDA UDI	Class I	Active
Xpress Minimally Invasive Pedicle Screw System	X073-0100-CR	FDA UDI	Class II	Active
Cortera Spinal Fixation System	150107-10090	FDA UDI	Class II	Active
Cortera Spinal Fixation System	150102-00040	FDA UDI	Class II	Active
Cortera Spinal Fixation System	1509-230110	FDA UDI	Class I	Active
X90 Pedicle Screw System	N605535SD-DL	FDA UDI	Class II	Active
Cortera Spinal Fixation System	150204-55110	FDA UDI	Class II	Active
Fortilink-A IBF System	65-A-S14-8L-TRL	FDA UDI	Class I	Unknown
Aranax Anterior Cervical Plating System	T086-1756	FDA UDI	Class I	Active
Irix-C Cervical Integrated Fusion System	X066-161308TP	FDA UDI	Class II	Active
Certex Spinal Fixation System	X067-1604	FDA UDI	Class II	Unknown
Calix Spinal Implant System	X034-0334	FDA UDI	Class II	Active
Axle Interspinous Fusion System	X060-1252	FDA UDI	Class II	Active
Contact ALP	25-60-24	FDA UDI	Class II	Active
Cortera Spinal Fixation System	150203-60135	FDA UDI	Class II	Active
Irix-A Lumbar Integrated Fusion System	X080-332615-16-STR	FDA UDI	Class II	Active
Calix Spinal Implant System	X034-1423	FDA UDI	Class II	Active
Xspan Laminoplasty Fixation System	X085-0308-H06-LU	FDA UDI	Class II	Active
Streamline OCT	26-OCPS-45-16	FDA UDI	Class II	Active
Irix-C Cervical Integrated Fusion System	X066-161307TL	FDA UDI	Class II	Active
Calix Spinal Implant System	X034-2781	FDA UDI	Class I	Active
Streamline® MIS Spinal Fixation System	04-TAP-50	FDA UDI	Class I	Unknown
Cortera	150151-90080	FDA UDI	Class II	Active
X90 Pedicle Screw System	N60000625-DL	FDA UDI	Class II	Active
Cortera	150100-25045	FDA UDI	Class II	Active
Xspan Laminoplasty Fixation System	X085-0310-F06-R	FDA UDI	Class II	Active
Certex Spinal Fixation System	X067-0875	FDA UDI	Class II	Unknown
Fortex Pedicle Screw System	X022-0110	FDA UDI	Class II	Active
Certex Spinal Fixation System	X067-1654	FDA UDI	Class II	Unknown
Cortera	150151-80095	FDA UDI	Class II	Active
Xpress Minimally Invasive Pedicle Screw System	X073-7570-DL	FDA UDI	Class II	Active
Xsert Lumbar Expandable Interbody System	T092-1400	FDA UDI	Class I	Unknown
X90 Pedicle Screw System	N607530SD	FDA UDI	Class II	Active
Calix Spinal Implant System	C034-0190	FDA UDI	Class I	Active
Axle Interspinous Fusion System	X060-0324	FDA UDI	Class I	Active
Axle Interspinous Fusion System	X060-0081	FDA UDI	Class II	Active
Xpress Minimally Invasive Pedicle Screw System	T073-1800	FDA UDI	Class I	Active
X90 Pedicle Screw System	N60000616-DL	FDA UDI	Class II	Active
nanOss 3D Advanced Bone Graft Substitute	90-300-25504	FDA UDI	Class II	Active
Calix Spinal Implant System	X034-0121	FDA UDI	Class II	Active
Cortera	150104-20105	FDA UDI	Class II	Active
Streamline TL Spinal Fixation System	01-RS-C-65-65	FDA UDI	Class II	Unknown
Streamline TL Spinal Fixation System	02-RACKDISTRACTOR	FDA UDI	Class I	Unknown
Fortex Pedicle Screw System	N60001101	FDA UDI	Class II	Active
Calix Spinal Implant System	X034-0240	FDA UDI	Class II	Active
Irix-A Lumbar Integrated Fusion System	X080-5535SD	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

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Authorities

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FDA Recalls (5)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Xtant Medical Holdings, Inc. has 5 recall records, with the earliest initiated on 2023-11-28 and the most recent on 2026-03-09. The statuses recorded are open and classified. The reasons given include incorrect labeling of shelf life, incorrect screw dimensions and labeling, incorrect expiration date, mislabeled part numbers, and implants marked 'DNI' that are not intended for implantation.

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
Mar 9, 2026	Z-1897-2026	—	open, classified	Products were incorrectly labeled with a 5-year shelf life. The approved and validated shelf life is four years.
Feb 18, 2026	Z-1773-2026	—	open, classified	Units from one lot were mislabeled with an incorrect part number, identifying the device as a shorter screw length than it physically is.
Jan 3, 2025	Z-1177-2025	—	open, classified	Certain implants in the Irix-A Lumbar Fusion System were distributed while labeled with an incorrect expiration date.
Aug 21, 2024	Z-0125-2025	—	open, classified	Spinal fixation system implant screws marked "DNI" are not intended to be implanted and may not have been manufactured in accordance with released manufacturing specifications, and if implanted the screws may not have adequate strength or performance.
Nov 28, 2023	Z-0846-2024	—	open, classified	Spinal fixation screws labeled as 8.5 mm diameter, 50 mm length were manufactured using an incorrect screw shank component, and so the labeling is incorrect because the affected screws are in fact 5.5 diameter, 45 mm length screws, which if used may lead to the screw not engaging.