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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 24 of 500

Device	Model / Reference	Registries	Class	Status
Brigade	1903354	FDA UDI	Class II	Active
ReLine	10245012	FDA UDI	Class II	Active
Acp	18002501	FDA UDI	Class II	Active
ReLine	16219080	FDA UDI	Class II	Active
CoRoent	1835684	FDA UDI	Class II	Active
CoRoent	5430358	FDA UDI	Class II	Active
ReLine	12460300	FDA UDI	Class II	Active
CoRoent	6910260P	FDA UDI	Class II	Active
Modulus	1982136	FDA UDI	Class I	Active
ReLine	24470060P	FDA UDI	Class I	Active
ReLine	14524585	FDA UDI	Class II	Active
ReLine	14521280	FDA UDI	Class II	Active
Modulus	1181050P2	FDA UDI	Class II	Active
CoRoent	5220325	FDA UDI	Class II	Active
ReLine	16460300	FDA UDI	Class II	Active
ReLine	12460090	FDA UDI	Class II	Active
ReLine	12450550	FDA UDI	Class II	Active
ReLine	13021111	FDA UDI	Class II	Active
Acp	8785120	FDA UDI	Class II	Active
ReLine	24029570	FDA UDI	Class II	Active
LateralALIF	1725197	FDA UDI	Class I	Active
CoRoent	5181302	FDA UDI	Class II	Active
ReLine	10200114	FDA UDI	Class II	Active
ReLine	16119575	FDA UDI	Class II	Active
Gradient	7461500	FDA UDI	Class II	Active
VuePoint	8975526	FDA UDI	Class II	Active
CoRoent	1713740	FDA UDI	Class II	Active
CoRoent	5195096	FDA UDI	Class II	Active
Helix	7741113	FDA UDI	Class II	Active
ReLine	24021535	FDA UDI	Class II	Active
Pgi	1667630	FDA UDI	Class I	Active
ReLine	14555035	FDA UDI	Class II	Active
ReLine	10245301	FDA UDI	Class II	Active
CoRoent	6481040P2	FDA UDI	Class II	Active
Precept	8837525A	FDA UDI	Class II	Active
Simplify	2-6EV-CE	FDA UDI	Class III	Active
CoRoent	1835737	FDA UDI	Class II	Active
LateralALIF	1725704	FDA UDI	Class I	Active
CoRoent	5220402	FDA UDI	Class II	Active
CoRoent	5129345	FDA UDI	Class II	Active
CoRoent	5209325	FDA UDI	Class II	Active
ReLine	11450170	FDA UDI	Class II	Active
ReLine	13116535	FDA UDI	Class II	Active
ReLine	16085535	FDA UDI	Class II	Active
CoRoent	5152308	FDA UDI	Class II	Active
Precept	8898535	FDA UDI	Class II	Active
CoRoent	5291282P2	FDA UDI	Class II	Active
CoRoent	7150950CP2	FDA UDI	Class II	Active
CoRoent	5434300	FDA UDI	Class II	Active
ReLine	13011145	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.