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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 5 of 500

Device	Model / Reference	Registries	Class	Status
Brigade	1903589	FDA UDI	Class II	Active
Brigade	1903410	FDA UDI	Class II	Active
CoRoent	5263302P2	FDA UDI	Class II	Active
ReLine	D10000939	FDA UDI	Class I	Active
ReLine	16116085	FDA UDI	Class II	Active
CoRoent	5123324	FDA UDI	Class II	Active
CoRoent	5154308	FDA UDI	Class II	Active
VuePoint	8975512	FDA UDI	Class II	Active
ReLine	13046060A	FDA UDI	Class II	Active
ReLine	16021125	FDA UDI	Class II	Active
CoRoent	1713609	FDA UDI	Class II	Active
CoRoent	5231344	FDA UDI	Class II	Active
ReLine	13031030	FDA UDI	Class II	Active
SpheRx	DB2IN2	FDA UDI	Class II	Active
ReLine	12155440	FDA UDI	Class II	Active
ReLine	12055470	FDA UDI	Class II	Active
Xlif	3224100	FDA UDI	Class I	Active
ReLine	11021570	FDA UDI	Class II	Active
MaXcess	1025461	FDA UDI	Class II	Active
ReLine	16211040	FDA UDI	Class II	Active
VuePoint	8980520P3	FDA UDI	Class II	Active
CoRoent	6216050CP2	FDA UDI	Class II	Active
CoRoent	1662615	FDA UDI	Class II	Active
CoRoent	5162282	FDA UDI	Class II	Active
ReLine	16081145	FDA UDI	Class II	Active
ReLine	14526095	FDA UDI	Class II	Active
CoRoent	5109344	FDA UDI	Class II	Active
ReLine	10200032	FDA UDI	Class II	Active
ReLine	3913536	FDA UDI	Class II	Active
CoRoent	5324402P2	FDA UDI	Class II	Active
CoRoent	1713630	FDA UDI	Class II	Active
ReLine	13055095A	FDA UDI	Class II	Active
CoRoent	5102325	FDA UDI	Class II	Active
CoRoent	5290362	FDA UDI	Class II	Active
CoRoent	5234284	FDA UDI	Class II	Active
ReLine	16016575	FDA UDI	Class II	Active
ReLine	13034540	FDA UDI	Class II	Active
ReLine	14360105	FDA UDI	Class II	Active
ReLine	10019555	FDA UDI	Class II	Active
CoRoent	5133342P2	FDA UDI	Class II	Active
CoRoent	5340250	FDA UDI	Class II	Active
VuePoint	8980336P	FDA UDI	Class II	Active
X-Core	7220067	FDA UDI	Class II	Active
Acp	18008323	FDA UDI	Class II	Active
Cohere	1960175	FDA UDI	Class II	Active
Pulse	50120101	FDA UDI	Class II	Active
ReLine	14545090	FDA UDI	Class II	Active
CoRoent	5293340P2	FDA UDI	Class II	Active
CoRoent	1713706	FDA UDI	Class II	Active
ReLine	13054010A	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.