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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 27 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	5202308P2	FDA UDI	Class II	Active
Acp	ACPIMP	FDA UDI	Class II	Active
CoRoent	5154320	FDA UDI	Class II	Active
ReLine	13045012A	FDA UDI	Class II	Active
ReLine	13011575	FDA UDI	Class II	Active
CoRoent	6310655006	FDA UDI	Class II	Active
ReLine	13035045	FDA UDI	Class II	Active
Apx	1672353	FDA UDI	Class II	Active
CoRoent	5240402	FDA UDI	Class II	Active
Archon	8880320	FDA UDI	Class II	Active
ReLine	11060065	FDA UDI	Class II	Active
ReLine	10015595	FDA UDI	Class II	Active
ReLine	3700211	FDA UDI	Class II	Active
CoRoent	5229285	FDA UDI	Class II	Active
ReLine	13085070	FDA UDI	Class II	Active
ReLine	10000687	FDA UDI	Class I	Active
CoRoent	6719106	FDA UDI	Class II	Active
Armada	8760530	FDA UDI	Class II	Active
Armada	8355030	FDA UDI	Class II	Active
CoRoent	6081035P	FDA UDI	Class II	Active
ReLine	13106550P	FDA UDI	Class II	Active
ReLine	11028512	FDA UDI	Class II	Active
ReLine	3704026	FDA UDI	Class II	Active
ReLine	16011065	FDA UDI	Class II	Active
Alif	6957066	FDA UDI	Class II	Active
CoRoent	6416250P2	FDA UDI	Class II	Active
Excavation	5155040	FDA UDI	Class I	Active
ReLine	14350140	FDA UDI	Class II	Active
ReLine	11360015	FDA UDI	Class II	Active
ReLine	10250208	FDA UDI	Class II	Active
ReLine	13044090A	FDA UDI	Class II	Active
ReLine	3795001	FDA UDI	Class I	Active
Cohere	8267860P2	FDA UDI	Class II	Active
ReLine	11000449	FDA UDI	Class II	Active
CoRoent	1903022	FDA UDI	Class II	Active
ReLine	10001133	FDA UDI	Class I	Active
CoRoent	5101364P2	FDA UDI	Class II	Active
Monolith	5991442	FDA UDI	Class II	Active
ReLine	RELILIACIMP	FDA UDI	Class II	Active
ReLine	11095530	FDA UDI	Class II	Active
Archon	8781611	FDA UDI	Class II	Active
ReLine	16177585	FDA UDI	Class II	Active
NuVasive	7510110	FDA UDI	Class I	Active
CoRoent	6091235P2	FDA UDI	Class II	Active
ReLine	10260118	FDA UDI	Class II	Active
CoRoent	5113344P2	FDA UDI	Class II	Active
ReLine	14518595	FDA UDI	Class II	Active
CoRoent	6809115	FDA UDI	Class II	Active
CoRoent	6009855P2	FDA UDI	Class II	Active
CoRoent	5191364P2	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.