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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 6 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	7150855P2	FDA UDI	Class II	Active
Tlx	1742649	FDA UDI	Class II	Active
ReLine	13187540	FDA UDI	Class II	Active
ReLine	14450025	FDA UDI	Class II	Active
CoRoent	5232340	FDA UDI	Class II	Active
CoRoent	5195167	FDA UDI	Class II	Active
ReLine	13039055	FDA UDI	Class II	Active
ReLine	10155030	FDA UDI	Class II	Active
CoRoent	6809714	FDA UDI	Class II	Active
CoRoent	6805115	FDA UDI	Class II	Active
ReLine	14150095	FDA UDI	Class II	Active
VuePoint	7907010	FDA UDI	Class I	Active
Armada	8447570	FDA UDI	Class II	Active
Acp	18009254	FDA UDI	Class II	Active
Acp	8786490	FDA UDI	Class II	Active
CoRoent	6725331	FDA UDI	Class II	Active
CoRoent	5384408	FDA UDI	Class II	Active
CoRoent	6733312	FDA UDI	Class II	Active
ReLine	12150230	FDA UDI	Class II	Active
ReLine	11255075	FDA UDI	Class II	Active
MaXcess	3220122	FDA UDI	Class I	Active
Mesh	1007636	FDA UDI	Class II	Active
MaXcess	1024681	FDA UDI	Class II	Active
ReLine	11019575	FDA UDI	Class II	Active
ReLine	10000022	FDA UDI	Class I	Active
ReLine	15155060	FDA UDI	Class II	Active
Armada	8992240	FDA UDI	Class I	Active
ReLine	12060350	FDA UDI	Class II	Active
Acp	18002233	FDA UDI	Class II	Active
ReLine	24350075	FDA UDI	Class I	Active
ReLine	3904532	FDA UDI	Class II	Active
Pulse	5050283	FDA UDI	Class II	Active
CoRoent	5151324	FDA UDI	Class II	Active
Simplify	2-6L-CE	FDA UDI	Class III	Active
ReLine	13386555P	FDA UDI	Class II	Active
ReLine	14424530P	FDA UDI	Class II	Active
ReLine	11000659	FDA UDI	Class I	Active
Brigade	1903393	FDA UDI	Class II	Active
CoRoent	5260324P2	FDA UDI	Class II	Active
CoRoent	5249304P2	FDA UDI	Class II	Active
CoRoent	5460304	FDA UDI	Class II	Active
ReLine	13189065	FDA UDI	Class II	Active
ReLine	16115570	FDA UDI	Class II	Active
ReLine	13054012	FDA UDI	Class II	Active
ReLine	24021540	FDA UDI	Class II	Active
ReLine	11011510	FDA UDI	Class II	Active
Brigade	1903315	FDA UDI	Class II	Active
ReLine	RELUNIIMP	FDA UDI	Class II	Active
ReLine	12455075	FDA UDI	Class II	Active
ReLine	13174545	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.