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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 23 of 500

Device	Model / Reference	Registries	Class	Status
Archon	8882593	FDA UDI	Class II	Active
Armada	8274530	FDA UDI	Class II	Active
ReLine	10016540	FDA UDI	Class II	Active
ReLine	10011185	FDA UDI	Class II	Active
ReLine	11360100P	FDA UDI	Class II	Active
Base	6954410	FDA UDI	Class II	Active
CoRoent	1618651	FDA UDI	Class II	Active
ReLine	12260580	FDA UDI	Class II	Active
ReLine	12250130	FDA UDI	Class II	Active
Armada	8355050	FDA UDI	Class II	Active
ReLine	10000364	FDA UDI	Class I	Active
VuePoint	7905514	FDA UDI	Class II	Active
Mas Plif	1581925	FDA UDI	Class I	Active
ReLine	13339570P	FDA UDI	Class II	Active
ReLine	3823528	FDA UDI	Class II	Active
ReLine	3804514	FDA UDI	Class II	Active
CoRoent	6990625	FDA UDI	Class II	Active
Halo	7876528	FDA UDI	Class II	Active
ReLine	10100019	FDA UDI	Class II	Active
Acp	1010677	FDA UDI	Class II	Active
ReLine	10012575	FDA UDI	Class II	Active
ReLine	13085525	FDA UDI	Class II	Active
ReLine	13028565	FDA UDI	Class II	Active
ReLine	12160380	FDA UDI	Class II	Active
ReLine	10000299	FDA UDI	Class I	Active
Acp	7573255	FDA UDI	Class II	Active
ReLine	11086011	FDA UDI	Class II	Active
Armada	7559145	FDA UDI	Class II	Active
ReLine	13107560P	FDA UDI	Class II	Active
ReLine	24029060	FDA UDI	Class II	Active
ReLine	3903545	FDA UDI	Class II	Active
ReLine	16115530	FDA UDI	Class II	Active
ReLine	10200307	FDA UDI	Class II	Active
ReLine	10245306	FDA UDI	Class II	Active
CoRoent	6041523P2	FDA UDI	Class II	Active
ReLine	14586520	FDA UDI	Class II	Active
Cohere	8181045P2	FDA UDI	Class II	Active
CoRoent	1903026	FDA UDI	Class II	Active
CoRoent	5144328P2	FDA UDI	Class II	Active
Modulus	1114345P2	FDA UDI	Class II	Active
ReLine	14514512	FDA UDI	Class II	Active
Archon	8781615	FDA UDI	Class II	Active
ReLine	16179525	FDA UDI	Class II	Active
ReLine	3776555	FDA UDI	Class II	Active
Archon	8781620	FDA UDI	Class II	Active
ReLine	10245033	FDA UDI	Class II	Active
ReLine	16118080	FDA UDI	Class II	Active
ReLine	16115055	FDA UDI	Class II	Active
Gradient	7440124	FDA UDI	Class II	Active
NuVasive	3300020	FDA UDI	Class I	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.