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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 11 of 500

Device	Model / Reference	Registries	Class	Status
Helix	7800352	FDA UDI	Class II	Active
ReLine	10070510	FDA UDI	Class II	Active
Cohere	1931348	FDA UDI	Class I	Active
ReLine	3790035	FDA UDI	Class I	Active
MaXcess	1542812	FDA UDI	Class I	Active
Acp	8785619	FDA UDI	Class II	Active
CoRoent	5219365	FDA UDI	Class II	Active
CoRoent	5484258	FDA UDI	Class II	Active
CoRoent	5271305	FDA UDI	Class II	Active
CoRoent	5394302	FDA UDI	Class II	Active
ReLine	16011211	FDA UDI	Class II	Active
XLIF Decade Plate	DECADEINS	FDA UDI	Class II	Active
ReLine	10000294	FDA UDI	Class I	Active
Armada	8450270	FDA UDI	Class II	Active
ReLine	12055400	FDA UDI	Class II	Active
ReLine	11025511	FDA UDI	Class II	Active
Archon	8881316	FDA UDI	Class II	Active
Precept	8809500AP	FDA UDI	Class II	Active
CoRoent	5251308P2	FDA UDI	Class II	Active
Archon	8780919	FDA UDI	Class II	Active
ReLine	11087560	FDA UDI	Class II	Active
Excavation	5155067	FDA UDI	Class I	Active
CoRoent	5150280P2	FDA UDI	Class II	Active
ReLine	10000688	FDA UDI	Class I	Active
Brigade	6968501	FDA UDI	Class II	Active
CoRoent	5152308P2	FDA UDI	Class II	Active
CoRoent	5282405P2	FDA UDI	Class II	Active
Xlif	LATCRESTLINE003	FDA UDI	Class II	Active
Halo Buttress Plate	7891023	FDA UDI	Class II	Active
CoRoent	6716926P2	FDA UDI	Class II	Active
ReLine	13181085	FDA UDI	Class II	Active
ReLine	13066560	FDA UDI	Class II	Active
CoRoent	6020001	FDA UDI	Class II	Active
ReLine	10011012	FDA UDI	Class II	Active
CoRoent	6300855	FDA UDI	Class II	Active
ReLine	11089010	FDA UDI	Class II	Active
ReLine	11086580	FDA UDI	Class II	Active
SpheRx	7767545	FDA UDI	Class II	Active
ReLine	1778558P	FDA UDI	Class I	Active
ReLine	3704550	FDA UDI	Class II	Active
ReLine	3960428	FDA UDI	Class II	Active
ReLine	3914042	FDA UDI	Class II	Active
ReLine	3837545	FDA UDI	Class II	Active
LessRay	1675899	FDA UDI	Class II	Active
Camber	8370030P	FDA UDI	Class II	Active
ReLine	3737055	FDA UDI	Class II	Active
CoRoent	5109322P2	FDA UDI	Class II	Active
CoRoent	5161325P2	FDA UDI	Class II	Active
Armada	8992202	FDA UDI	Class I	Active
CoRoent	5281345P2	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.