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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 19 of 500

Device	Model / Reference	Registries	Class	Status
ReLine	13179090	FDA UDI	Class II	Active
CoRoent	5152400	FDA UDI	Class II	Active
CoRoent	5259344	FDA UDI	Class II	Active
ReLine	16085585	FDA UDI	Class II	Active
ReLine	16029095	FDA UDI	Class II	Active
ReLine	13021190	FDA UDI	Class II	Active
Armada	7459255	FDA UDI	Class II	Active
SpheRx	7248585	FDA UDI	Class II	Active
CoRoent	6208165	FDA UDI	Class II	Active
CoRoent	6814815	FDA UDI	Class II	Active
ReLine	11026585	FDA UDI	Class II	Active
Modulus	1081302P2	FDA UDI	Class II	Active
Alif	6956961	FDA UDI	Class II	Active
ReLine	10001247	FDA UDI	Class I	Active
CoRoent	5124344	FDA UDI	Class II	Active
CoRoent	6922088	FDA UDI	Class II	Active
ReLine	15150180	FDA UDI	Class II	Active
VuePoint	8980538P3	FDA UDI	Class II	Active
CoRoent	5163285	FDA UDI	Class II	Active
CoRoent	5151340	FDA UDI	Class II	Active
ReLine	16085085	FDA UDI	Class II	Active
ReLine	16026510	FDA UDI	Class II	Active
Acp	18009510	FDA UDI	Class II	Active
MaXcess	1552333	FDA UDI	Class I	Active
ReLine	3745050	FDA UDI	Class II	Active
ReLine	3943070	FDA UDI	Class II	Active
ReLine	3900506	FDA UDI	Class II	Active
ReLine	3990245	FDA UDI	Class II	Active
ReLine	3836030	FDA UDI	Class II	Active
NuVasive	Z200222-008	FDA UDI	Class II	Active
CoRoent	5203362P2	FDA UDI	Class II	Active
Modulus	1921041P2	FDA UDI	Class II	Active
ReLine	3741400	FDA UDI	Class II	Active
Cohere	3141404	FDA UDI	Class I	Active
ReLine	3900305	FDA UDI	Class II	Active
ReLine	24010511	FDA UDI	Class II	Active
Acp	18006461	FDA UDI	Class II	Active
VuePoint	8976147	FDA UDI	Class II	Active
ReLine	16214590	FDA UDI	Class II	Active
ReLine	16215540	FDA UDI	Class II	Active
CoRoent	6777014	FDA UDI	Class II	Active
CoRoent	6214160CP2	FDA UDI	Class II	Active
CoRoent	6108925P2	FDA UDI	Class II	Active
CoRoent	5380302P2	FDA UDI	Class II	Active
ReLine	13119025	FDA UDI	Class II	Active
CoRoent	5163344	FDA UDI	Class II	Active
CoRoent	5119400	FDA UDI	Class II	Active
ReLine	16085012	FDA UDI	Class II	Active
ReLine	16026035	FDA UDI	Class II	Active
ReLine	13055585	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.