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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 25 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	6510255P2	FDA UDI	Class II	Active
ReLine	13185070	FDA UDI	Class II	Active
ReLine	13180560	FDA UDI	Class II	Active
ReLine	24019090	FDA UDI	Class II	Active
ReLine	14218040	FDA UDI	Class II	Active
CoRoent	5299340P2	FDA UDI	Class II	Active
CoRoent	5259280P2	FDA UDI	Class II	Active
Alif	6956984	FDA UDI	Class II	Active
CoRoent	6776011	FDA UDI	Class II	Active
CoRoent	6212065CP2	FDA UDI	Class II	Active
CoRoent	5420254	FDA UDI	Class II	Active
CoRoent	5184345	FDA UDI	Class II	Active
ReLine	10101212	FDA UDI	Class II	Active
ReLine	13065010	FDA UDI	Class II	Active
SpheRx	7247595	FDA UDI	Class II	Active
Pgi	7101041	FDA UDI	Class I	Active
Xlif	1632768	FDA UDI	Class I	Active
NuVasive	3300608	FDA UDI	Class I	Active
ReLine	3790012	FDA UDI	Class I	Active
ReLine	3742070	FDA UDI	Class II	Active
CoRoent	5153404P2	FDA UDI	Class II	Active
ReLine	14610585	FDA UDI	Class II	Active
ReLine	3796265	FDA UDI	Class II	Active
Traverse	7867525	FDA UDI	Class II	Active
Traverse	7830011	FDA UDI	Class II	Active
CoRoent	6011328P2	FDA UDI	Class II	Active
Modulus	1265914	FDA UDI	Class II	Active
CoRoent	5269348P2	FDA UDI	Class II	Active
CoRoent	5231405P2	FDA UDI	Class II	Active
ReLine	13185585	FDA UDI	Class II	Active
ReLine	13081245	FDA UDI	Class II	Active
CoRoent	6851111	FDA UDI	Class II	Active
Radian	FACSIN	FDA UDI	Class II	Active
CoRoent	6200002	FDA UDI	Class I	Active
ReLine	3913534	FDA UDI	Class II	Active
ReLine	10001202	FDA UDI	Class I	Active
CoRoent	5164282	FDA UDI	Class II	Active
ReLine	15455090	FDA UDI	Class II	Active
ReLine	16081235	FDA UDI	Class II	Active
ReLine	16029040	FDA UDI	Class II	Active
NuVasive	Z500116-112	FDA UDI	Class II	Active
Acp	8785119	FDA UDI	Class II	Active
MaXcess	XALIFACCESS	FDA UDI	Class II	Active
ReLine	2200306	FDA UDI	Class I	Active
Xlif	1910112P2	FDA UDI	Class II	Active
ReLine	3835554	FDA UDI	Class II	Active
CoRoent	5190305P2	FDA UDI	Class II	Active
CoRoent	5182360P2	FDA UDI	Class II	Active
ReLine	2200503	FDA UDI	Class I	Active
CoRoent	5291304P2	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.