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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 10 of 500

Device	Model / Reference	Registries	Class	Status
CoRoent	5103342	FDA UDI	Class II	Active
CoRoent	5291325	FDA UDI	Class II	Active
ReLine	16017030	FDA UDI	Class II	Active
ReLine	13064045	FDA UDI	Class II	Active
Armada	8745540	FDA UDI	Class II	Active
CoRoent	6015640006	FDA UDI	Class II	Active
ReLine	11028550	FDA UDI	Class II	Active
ReLine	3764012	FDA UDI	Class II	Active
ReLine	3936530	FDA UDI	Class II	Active
Armada	7559309	FDA UDI	Class II	Active
ReLine	3835058	FDA UDI	Class II	Active
CoRoent	6150828	FDA UDI	Class II	Active
CoRoent	5182364	FDA UDI	Class II	Active
ReLine	13065080	FDA UDI	Class II	Active
CoRoent	5150288	FDA UDI	Class II	Active
Armada	8546560	FDA UDI	Class II	Active
CoRoent	1713647	FDA UDI	Class II	Active
CoRoent	5121308P2	FDA UDI	Class II	Active
ReLine	13218585	FDA UDI	Class II	Active
Brigade	6981034	FDA UDI	Class II	Active
CoRoent	5200365	FDA UDI	Class II	Active
CoRoent	5334308	FDA UDI	Class II	Active
ReLine	10000172	FDA UDI	Class I	Active
ReLine	14455135	FDA UDI	Class II	Active
CoRoent	6221845	FDA UDI	Class II	Active
Apx	1632872	FDA UDI	Class II	Active
ReLine	10050055	FDA UDI	Class II	Active
Nvm5	1582845	FDA UDI	Class II	Active
ReLine	16316545P	FDA UDI	Class II	Active
AttraX	5015104	FDA UDI	Class II	Active
Alif	6957036	FDA UDI	Class II	Active
CoRoent	5184360P2	FDA UDI	Class II	Active
ReLine	14581545	FDA UDI	Class II	Active
Mas Plif	3540015	FDA UDI	Class I	Active
Archon	8780515	FDA UDI	Class II	Active
Nvm5	1559165	FDA UDI	Class II	Active
ReLine	14355030P	FDA UDI	Class II	Active
ReLine	3744115	FDA UDI	Class II	Active
ReLine	10300909P	FDA UDI	Class II	Active
Acp	18008523	FDA UDI	Class II	Active
ReLine	3764520	FDA UDI	Class II	Active
CoRoent	5410354	FDA UDI	Class II	Active
CoRoent	5434252	FDA UDI	Class II	Active
CoRoent	5113408	FDA UDI	Class II	Active
CoRoent	7211245	FDA UDI	Class II	Active
Cohere	D1814394	FDA UDI	Class II	Active
Acp	8789244	FDA UDI	Class II	Active
ReLine	12060130	FDA UDI	Class II	Active
Brigade	7806522	FDA UDI	Class II	Active
CoRoent	7871250	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.