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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 9 of 500

Device	Model / Reference	Registries	Class	Status
ReLine	16186040	FDA UDI	Class II	Active
ReLine	13022545	FDA UDI	Class II	Active
ReLine	D10000803	FDA UDI	Class II	Active
ReLine	15355330	FDA UDI	Class II	Active
SpheRx	7248120	FDA UDI	Class II	Active
ReLine	15250550	FDA UDI	Class II	Active
Brigade	1903509	FDA UDI	Class II	Active
Brigade	1903329	FDA UDI	Class II	Active
CoRoent	5195384	FDA UDI	Class II	Active
ReLine	14528555	FDA UDI	Class II	Active
ReLine	14526550	FDA UDI	Class II	Active
ReLine	10200616	FDA UDI	Class II	Active
Nvm5	1712020	FDA UDI	Class I	Active
ReLine	16110535	FDA UDI	Class II	Active
ReLine	13176580	FDA UDI	Class II	Active
ReLine	15160540	FDA UDI	Class II	Active
NuVasive	Z700193-30	FDA UDI	Class II	Active
CoRoent	6793119	FDA UDI	Class II	Active
ReLine	16215070	FDA UDI	Class II	Active
CoRoent	6777209	FDA UDI	Class II	Active
CoRoent	6774107	FDA UDI	Class II	Active
ReLine	14528010	FDA UDI	Class II	Active
Modulus	1221845P2	FDA UDI	Class II	Active
CoRoent	5192302	FDA UDI	Class II	Active
CoRoent	5354308	FDA UDI	Class II	Active
SpheRx	7375555	FDA UDI	Class II	Active
Brigade	6921634	FDA UDI	Class II	Active
NuVasive	6904433	FDA UDI	Class I	Active
Precept	8848120	FDA UDI	Class II	Active
ReLine	15150130	FDA UDI	Class II	Active
ReLine	3790047	FDA UDI	Class I	Active
ReLine	3749113	FDA UDI	Class II	Active
Mas Plif	7125525	FDA UDI	Class II	Active
CoRoent	5201340P2	FDA UDI	Class II	Active
Acp	8786501	FDA UDI	Class II	Active
CoRoent	5120342P2	FDA UDI	Class II	Active
Modulus	1300405	FDA UDI	Class I	Active
NuVasive	4210140	FDA UDI	Class II	Active
CoRoent	5284328P2	FDA UDI	Class II	Active
Precept	8899545	FDA UDI	Class II	Active
ReLine	11036540	FDA UDI	Class II	Active
Tlif	6602009	FDA UDI	Class II	Active
CoRoent	5485535	FDA UDI	Class II	Active
ReLine	13319565P	FDA UDI	Class II	Active
ReLine	13314045P	FDA UDI	Class II	Active
CoRoent	5153300P2	FDA UDI	Class II	Active
ReLine	21447035	FDA UDI	Class II	Active
ReLine	14519050	FDA UDI	Class II	Active
CoRoent	6921660CP2	FDA UDI	Class II	Active
ReLine	13180545	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.