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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 30 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	6120928	FDA UDI	Class II	Active
MaXcess	3242130	FDA UDI	Class I	Active
ReLine	16111025	FDA UDI	Class II	Active
CoRoent	5210320	FDA UDI	Class II	Active
Xlp	7522006	FDA UDI	Class II	Active
Brigade	6968506	FDA UDI	Class II	Active
Brigade	6967134	FDA UDI	Class II	Active
Brigade	1903473	FDA UDI	Class II	Active
ReLine	14581170	FDA UDI	Class II	Active
ReLine	14586080	FDA UDI	Class II	Active
Alif	6957040	FDA UDI	Class II	Active
CoRoent	1835688	FDA UDI	Class II	Active
ReLine	14515510	FDA UDI	Class II	Active
ReLine	13191111	FDA UDI	Class II	Active
ReLine	13066512	FDA UDI	Class II	Active
ReLine	11155195	FDA UDI	Class II	Active
ReLine	11155100	FDA UDI	Class II	Active
ReLine	14417580P	FDA UDI	Class II	Active
CoRoent	5223325P2	FDA UDI	Class II	Active
ReLine	13017035	FDA UDI	Class II	Active
ReLine	14350125	FDA UDI	Class II	Active
CoRoent	5410402	FDA UDI	Class II	Active
CoRoent	6711926	FDA UDI	Class II	Active
CoRoent	6109130	FDA UDI	Class II	Active
ReLine	11038045	FDA UDI	Class II	Active
VuePoint	7904514	FDA UDI	Class II	Active
Mas Plif	7242060	FDA UDI	Class II	Active
ReLine	12155470	FDA UDI	Class II	Active
Traverse	7856530	FDA UDI	Class II	Active
ReLine	11017025	FDA UDI	Class II	Active
VuePoint	7906314	FDA UDI	Class II	Active
ReLine	3787526	FDA UDI	Class II	Active
ReLine	14526085	FDA UDI	Class II	Active
CoRoent	6920860CP2	FDA UDI	Class II	Active
CoRoent	6480945P2	FDA UDI	Class II	Active
ReLine	14528090	FDA UDI	Class II	Active
CoRoent	5169325	FDA UDI	Class II	Active
CoRoent	5211348	FDA UDI	Class II	Active
CoRoent	5152408	FDA UDI	Class II	Active
CoRoent	5221402	FDA UDI	Class II	Active
ReLine	14555570	FDA UDI	Class II	Active
ReLine	14546550	FDA UDI	Class II	Active
Tlx	1775120	FDA UDI	Class II	Active
Mlx	3321830	FDA UDI	Class I	Active
ReLine	14521210	FDA UDI	Class II	Active
CoRoent	5110284	FDA UDI	Class II	Active
VuePoint	8975510	FDA UDI	Class II	Active
ReLine	14460110	FDA UDI	Class II	Active
ReLine	16085010	FDA UDI	Class II	Active
ReLine	11044530	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.