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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 21 of 500

Device	Model / Reference	Registries	Class	Status
ReLine	14589530	FDA UDI	Class II	Active
CoRoent	5192408P2	FDA UDI	Class II	Active
ReLine	3890006	FDA UDI	Class I	Active
CoRoent	5189304P2	FDA UDI	Class II	Active
CoRoent	6480855	FDA UDI	Class II	Active
ReLine	13218575	FDA UDI	Class II	Active
CoRoent	6251212	FDA UDI	Class I	Active
ReLine	11160185	FDA UDI	Class II	Active
Precept	8809545A	FDA UDI	Class II	Active
Acp	8789230	FDA UDI	Class II	Active
ReLine	3736552	FDA UDI	Class II	Active
ReLine	10000099	FDA UDI	Class I	Active
Xlx	D1871500	FDA UDI	Class II	Active
ReLine	14514540	FDA UDI	Class II	Active
CoRoent	6041328P2	FDA UDI	Class II	Active
Archon	8781623	FDA UDI	Class II	Active
Archon	8780716	FDA UDI	Class II	Active
Excavation	5155192	FDA UDI	Class I	Active
NuVasive	Z700250-05	FDA UDI	Class I	Active
Tlx	5905336P2	FDA UDI	Class II	Active
CoRoent	5121404P2	FDA UDI	Class II	Active
ReLine	21447030	FDA UDI	Class II	Active
ReLine	14544511	FDA UDI	Class II	Active
ReLine	16179040	FDA UDI	Class II	Active
ReLine	17460500	FDA UDI	Class II	Active
CoRoent	5261304P2	FDA UDI	Class II	Active
ReLine	15250490	FDA UDI	Class II	Active
ReLine	24027520	FDA UDI	Class II	Active
ReLine	11081135	FDA UDI	Class II	Active
ReLine	14444030P	FDA UDI	Class II	Active
ReLine	14116550P	FDA UDI	Class II	Active
CoRoent	1662329	FDA UDI	Class II	Active
CoRoent	5224304	FDA UDI	Class II	Active
ReLine	16088045	FDA UDI	Class II	Active
ReLine	3746600	FDA UDI	Class II	Active
CoRoent	5111325P2	FDA UDI	Class II	Active
Cohere	8181060P2	FDA UDI	Class II	Active
CoRoent	5163308P2	FDA UDI	Class II	Active
Brigade	6968450	FDA UDI	Class II	Active
ReLine	3837054	FDA UDI	Class II	Active
CoRoent	6647926	FDA UDI	Class II	Active
ReLine	12150170	FDA UDI	Class II	Active
SpheRx	4486530	FDA UDI	Class II	Active
ReLine	11084575	FDA UDI	Class II	Active
ReLine	D1642994	FDA UDI	Class II	Active
CoRoent	5133285P2	FDA UDI	Class II	Active
ReLine	11010234	FDA UDI	Class II	Active
Armada	8436595	FDA UDI	Class II	Active
Precept	8890003	FDA UDI	Class II	Active
MaXcess	1559184	FDA UDI	Class I	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.