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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 32 of 500

Device	Model / Reference	Registries	Class	Status
VuePoint	8976112P	FDA UDI	Class II	Active
ReLine	15455180	FDA UDI	Class II	Active
CoRoent	5191364	FDA UDI	Class II	Active
ReLine	16081285	FDA UDI	Class II	Active
SpheRx	7376550	FDA UDI	Class II	Active
ReLine	13346035P	FDA UDI	Class II	Active
Triad	1011635	FDA UDI	Class I	Active
ReLine	13318580P	FDA UDI	Class II	Active
ReLine	11014025	FDA UDI	Class II	Active
ReLine	11000779	FDA UDI	Class I	Active
Acp	18006512	FDA UDI	Class II	Active
VuePoint	8980346P	FDA UDI	Class II	Active
ReLine	13227560P	FDA UDI	Class II	Active
ReLine	1001813	FDA UDI	Class I	Active
CoRoent	5291284P2	FDA UDI	Class II	Active
CoRoent	6778707CP2	FDA UDI	Class II	Active
CoRoent	6051328P2	FDA UDI	Class II	Active
CoRoent	5262282	FDA UDI	Class II	Active
CoRoent	5262304	FDA UDI	Class II	Active
CoRoent	5249288	FDA UDI	Class II	Active
ReLine	16021145	FDA UDI	Class II	Active
ReLine	13089570	FDA UDI	Class II	Active
Precept	8830540A	FDA UDI	Class II	Active
ReLine	15150460	FDA UDI	Class II	Active
ReLine	11025545	FDA UDI	Class II	Active
SpheRx	7754555	FDA UDI	Class II	Active
ReLine	10000686	FDA UDI	Class I	Active
Xlif	6940018	FDA UDI	Class I	Active
CoRoent	6703213	FDA UDI	Class I	Active
ReLine	15155030	FDA UDI	Class II	Active
X-Core	D5961400	FDA UDI	Class II	Active
CoRoent	5144285P2	FDA UDI	Class II	Active
ReLine	RELGATORIN	FDA UDI	Class II	Active
ReLine	11010319	FDA UDI	Class II	Active
Precept	8837560A	FDA UDI	Class II	Active
CoRoent	5430258	FDA UDI	Class II	Active
CoRoent	5184324	FDA UDI	Class II	Active
ReLine	13044565	FDA UDI	Class II	Active
CoRoent	5450155	FDA UDI	Class I	Active
ReLine	10025535	FDA UDI	Class II	Active
ReLine	3784525	FDA UDI	Class II	Active
ReLine	11011211	FDA UDI	Class II	Active
ReLine	13319535P	FDA UDI	Class II	Active
ReLine	10077540	FDA UDI	Class II	Active
ReLine	12055340	FDA UDI	Class II	Active
ReLine	10012545	FDA UDI	Class II	Active
CoRoent	5181404	FDA UDI	Class II	Active
Archon	8880523	FDA UDI	Class II	Active
ReLine	3714018	FDA UDI	Class II	Active
MaXcess	1560061	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.