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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 31 of 500

Device	Model / Reference	Registries	Class	Status
VuePoint	8976352	FDA UDI	Class II	Active
ReLine	14522540	FDA UDI	Class II	Active
ReLine	13188540	FDA UDI	Class II	Active
ReLine	13219595	FDA UDI	Class II	Active
CoRoent	5219322	FDA UDI	Class II	Active
CoRoent	5350354	FDA UDI	Class II	Active
ReLine	12460025	FDA UDI	Class II	Active
ReLine	11450080	FDA UDI	Class II	Active
CoRoent	5182404	FDA UDI	Class II	Active
ReLine	16021550	FDA UDI	Class II	Active
CoRoent	5143408	FDA UDI	Class II	Active
CoRoent	6851416	FDA UDI	Class II	Active
Precept	8834545B	FDA UDI	Class II	Active
CoRoent	6108925	FDA UDI	Class II	Active
ReLine	24036030	FDA UDI	Class II	Active
Acp	18006236	FDA UDI	Class II	Active
ReLine	24018560	FDA UDI	Class II	Active
ReLine	3900326	FDA UDI	Class II	Active
Pulse	1802417	FDA UDI	Class II	Active
Cohere	1964430P2	FDA UDI	Class II	Active
ReLine	1200009	FDA UDI	Class I	Active
ReLine	10000769	FDA UDI	Class I	Active
Xlif	6940005	FDA UDI	Class I	Active
ReLine	12350085	FDA UDI	Class II	Active
ReLine	10077070	FDA UDI	Class II	Active
VuePoint	7903003	FDA UDI	Class II	Active
Helix	7804215	FDA UDI	Class II	Active
ReLine	14414420P	FDA UDI	Class II	Active
ReLine	10145320P	FDA UDI	Class II	Active
ReLine	3741100	FDA UDI	Class II	Active
CoRoent	5203320P2	FDA UDI	Class II	Active
ReLine	3824550	FDA UDI	Class II	Active
Cohere	1982025P2	FDA UDI	Class II	Active
NuVasive	Z700224-07	FDA UDI	Class II	Active
CoRoent	5291280P2	FDA UDI	Class II	Active
CoRoent	5261348P2	FDA UDI	Class II	Active
ReLine	RSSCOREIN1	FDA UDI	Class II	Active
CoRoent	1835720	FDA UDI	Class II	Active
CoRoent	5133345	FDA UDI	Class II	Active
CoRoent	6771230CP2	FDA UDI	Class II	Active
ReLine	10100911	FDA UDI	Class II	Active
Xlif	1781920	FDA UDI	Class I	Active
ReLine	13055050	FDA UDI	Class II	Active
ReLine	13019580	FDA UDI	Class II	Active
ReLine	15350050	FDA UDI	Class II	Active
CoRoent	5476525	FDA UDI	Class II	Active
ReLine	12155520	FDA UDI	Class II	Active
CoRoent	7870855	FDA UDI	Class II	Active
Brigade	1903593	FDA UDI	Class II	Active
ReLine	16216585	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.