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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 18 of 500

Device	Model / Reference	Registries	Class	Status
ReLine	ALPRELHSIM	FDA UDI	Class II	Active
MaXcess	3500017	FDA UDI	Class II	Active
ReLine	11000425	FDA UDI	Class I	Active
ReLine	14511585	FDA UDI	Class II	Active
NuVasive Power	NUVAPOWERBAT	FDA UDI	Class II	Active
ReLine	16086040	FDA UDI	Class II	Active
Mlx	3321827	FDA UDI	Class I	Active
ReLine	11081045	FDA UDI	Class II	Active
CoRoent	5212340	FDA UDI	Class II	Active
ReLine	12460600	FDA UDI	Class II	Active
ReLine	16020545	FDA UDI	Class II	Active
CoRoent	5139284	FDA UDI	Class II	Active
SpheRx	7248035	FDA UDI	Class II	Active
Armada	8554030	FDA UDI	Class II	Active
ReLine	3937035	FDA UDI	Class II	Active
ReLine	3741450	FDA UDI	Class II	Active
ReLine	16089035	FDA UDI	Class II	Active
CoRoent	1644430	FDA UDI	Class I	Active
ReLine	13055011	FDA UDI	Class II	Active
ReLine	13034030	FDA UDI	Class II	Active
ReLine	13028040	FDA UDI	Class II	Active
Precept	8827530	FDA UDI	Class II	Active
CoRoent	6812840	FDA UDI	Class II	Active
X-Core	5961001	FDA UDI	Class II	Active
ReLine	12255020	FDA UDI	Class II	Active
VuePoint	7906007	FDA UDI	Class II	Active
ReLine	11011050	FDA UDI	Class II	Active
Pcm	7673002	FDA UDI	Class III	Active
VuePoint	8794524	FDA UDI	Class II	Active
Armada	8756055	FDA UDI	Class II	Active
SpheRx	7782200	FDA UDI	Class II	Active
ReLine	12600000P	FDA UDI	Class II	Active
Tlx	5881400	FDA UDI	Class II	Active
Base	6959266	FDA UDI	Class II	Active
CoRoent	6009660006	FDA UDI	Class II	Active
CoRoent	5224340	FDA UDI	Class II	Active
ReLine	13089010	FDA UDI	Class II	Active
ReLine	10000817	FDA UDI	Class II	Active
ReLine	14355035	FDA UDI	Class II	Active
ReLine	D10000583	FDA UDI	Class I	Active
ReLine	3824044	FDA UDI	Class II	Active
Xlif	6910103	FDA UDI	Class I	Active
CoRoent	6840100	FDA UDI	Class I	Active
VuePoint	7902312	FDA UDI	Class II	Active
CoRoent	6600053	FDA UDI	Class II	Active
Alif	6971012	FDA UDI	Class I	Active
Acp	8789240	FDA UDI	Class II	Active
Modulus	1265928	FDA UDI	Class II	Active
CoRoent	5259300P2	FDA UDI	Class II	Active
CoRoent	5221362	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.