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Nuvasive, Inc.

United States·US-MF-000007421

Last updated September 17, 2026

Information

Country: United States
Address: 7475, Lusk Blvd, San Diego, United States
Website: https://www.globusmedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: +1-858-909-1800
PRRC Contact: Daniel S. Paul
EUDAMED SRN: US-MF-000007421
FDA FEI Number: 3002980729
DUNS Number: 053950783

Catalogue (44291)

Page 14 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	5350402P2	FDA UDI	Class II	Active
CoRoent	CRVINTHLIMP20	FDA UDI	Class II	Active
ReLine	13057565	FDA UDI	Class II	Active
CoRoent	5290305	FDA UDI	Class II	Active
ReLine	11460045	FDA UDI	Class II	Active
ReLine	13110590	FDA UDI	Class II	Active
CoRoent	5113348	FDA UDI	Class II	Active
ReLine	14150135	FDA UDI	Class II	Active
Modulus	1921067P2	FDA UDI	Class II	Active
Brigade	1903431	FDA UDI	Class II	Active
Excavation	5155011	FDA UDI	Class I	Active
CoRoent	1625549	FDA UDI	Class II	Active
ReLine	10072550	FDA UDI	Class II	Active
MaXcess	1610014	FDA UDI	Class I	Active
SpheRx	7284530	FDA UDI	Class II	Active
ReLine	15150470	FDA UDI	Class II	Active
CoRoent	6011212	FDA UDI	Class II	Active
ReLine	14255115	FDA UDI	Class II	Active
Armada	8452356	FDA UDI	Class II	Active
NuVasive	3200107	FDA UDI	Class I	Active
VuePoint	7903144	FDA UDI	Class II	Active
VuePoint	7902416	FDA UDI	Class II	Active
ReLine	11018575	FDA UDI	Class II	Active
ReLine	14218545	FDA UDI	Class II	Active
CoRoent	6512260CP2	FDA UDI	Class II	Active
LateralALIF	1725729	FDA UDI	Class I	Active
LateralALIF	1725002	FDA UDI	Class I	Active
CoRoent	5204282	FDA UDI	Class II	Active
ReLine	15160490	FDA UDI	Class II	Active
Precept	8806535	FDA UDI	Class II	Active
CoRoent	1618428	FDA UDI	Class II	Active
X-Core	6185000	FDA UDI	Class II	Active
ReLine	11026512	FDA UDI	Class II	Active
Cohere	1982010P2	FDA UDI	Class II	Active
CoRoent	5182280P2	FDA UDI	Class II	Active
CoRoent	5104345P2	FDA UDI	Class II	Active
VuePoint	8975634	FDA UDI	Class II	Active
MaXcess	1558472	FDA UDI	Class II	Active
ReLine	15260380	FDA UDI	Class II	Active
ReLine	3735526	FDA UDI	Class II	Active
ReLine	3790003	FDA UDI	Class I	Active
Modulus	MDLUSALIFTRIAL3428	FDA UDI	Class II	Active
Acp	18009462	FDA UDI	Class II	Active
Base	6959104	FDA UDI	Class II	Active
CoRoent	6733307	FDA UDI	Class II	Active
ReLine	12355160	FDA UDI	Class II	Active
NuVasive	7240041	FDA UDI	Class I	Active
Brigade	1638271	FDA UDI	Class I	Active
Armada	8439580	FDA UDI	Class II	Active
CoRoent	6121123P	FDA UDI	Class II	Active

Related Companies

Authorised Representatives

AJW Technology Consulting GmbH DE

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (36)

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

Date	Recall No.	Class	Status	Reason
Nov 10, 2022	Z-0738-2023	—	open, classified	Potential that insert will be unable to disengage from the vertebral body replacement device/implant
Jul 19, 2022	Z-1052-2023	—	open, classified	Due to an incorrect security key, customers were unable to connect to remote monitoring during spinal surgery, neck dissections, thoracic surgeries, and upper and lower extremity procedures.
Jun 20, 2022	Z-1453-2022	—	open, classified	Cervical artificial disc Unique Device Identifier (UDI) barcodes contain the incorrect Global Trade Item Number (GTIN) on the Patient Label when scanned and may also contain the incorrect GTIN human readable text, which could lead to selecting an incorrectly sized unit.
Jun 10, 2020	Z-2684-2020	—	terminated	The NVM5 EMG Module kit intended for intraoperative neurophysiologic monitoring during spinal surgery contains incorrect component, part number 1715945, SSEP harness instead of the the correct part number 1747065, NVM5 Harness, Gen 3.5 EM. This issue can result in delay in therapy or lack of EMG neuromonitoring during surgery if the surgeon elects to proceed without the NVM5.
Feb 13, 2020	Z-1898-2020	—	terminated	Post-implantation separation of an actuator end cap component that may expose internal components of the actuator, which could lead to hastened degeneration of the internal components and egress of Titanium alloy wear debris and resultant localized tissue discoloration.
Jan 5, 2009	Z-0369-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0361-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0351-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0370-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0375-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0348-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0354-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0377-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0355-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0374-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0378-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0352-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0372-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0363-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0350-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0364-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0367-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0359-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0366-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0373-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0362-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0349-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0360-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0353-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0365-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0376-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0371-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0357-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0358-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0368-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.
Jan 5, 2009	Z-0356-2013	—	terminated	The tulip portion of the screw assembly can disengage from the shank after implantation.