Is this your brand? Sign in to claim ownership.

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 13 of 500

Device	Model / Reference	Registries	Class	Status
Traverse	7821050	FDA UDI	Class II	Active
ReLine	10077595	FDA UDI	Class II	Active
ReLine	10017045	FDA UDI	Class II	Active
ReLine	10011595	FDA UDI	Class II	Active
ReLine	13337560P	FDA UDI	Class II	Active
CoRoent	6015235	FDA UDI	Class II	Active
VuePoint	8980136P	FDA UDI	Class II	Active
Acp	8789237	FDA UDI	Class II	Active
ReLine	14516510	FDA UDI	Class II	Active
Monolith	5995165	FDA UDI	Class I	Active
CoRoent	6301055	FDA UDI	Class II	Active
ReLine	10079590	FDA UDI	Class II	Active
ReLine	14455530P	FDA UDI	Class II	Active
ReLine	3702535	FDA UDI	Class II	Active
Armada	8255540	FDA UDI	Class II	Active
ReLine	10015055	FDA UDI	Class II	Active
ReLine	24028085	FDA UDI	Class II	Active
ReLine	16211090	FDA UDI	Class II	Active
CoRoent	5360354P2	FDA UDI	Class II	Active
CoRoent	5310254P2	FDA UDI	Class II	Active
CoRoent	5404252	FDA UDI	Class II	Active
CoRoent	5151344	FDA UDI	Class II	Active
Precept	8848130	FDA UDI	Class II	Active
Brigade	8555325	FDA UDI	Class II	Active
ReLine	15150140	FDA UDI	Class II	Active
Mas Plif	3540011	FDA UDI	Class I	Active
ReLine	BETRELCNAVS	FDA UDI	Class II	Active
ReLine	14360060P	FDA UDI	Class II	Active
VuePoint	8975632	FDA UDI	Class II	Active
MaXcess	1558646	FDA UDI	Class I	Active
ReLine	3704018	FDA UDI	Class II	Active
ReLine	24011135	FDA UDI	Class II	Active
CoRoent	6774711	FDA UDI	Class II	Active
Xlif	6996112	FDA UDI	Class I	Active
CoRoent	5249302P2	FDA UDI	Class II	Active
CoRoent	7161540	FDA UDI	Class II	Active
ReLine	10001028	FDA UDI	Class II	Active
CoRoent	1657328	FDA UDI	Class II	Active
ReLine	16018530	FDA UDI	Class II	Active
Armada	8992116	FDA UDI	Class I	Active
Armada	8745045	FDA UDI	Class II	Active
Precept	8887002	FDA UDI	Class II	Active
CoRoent	6170855	FDA UDI	Class II	Active
Armada	8453114	FDA UDI	Class II	Active
ReLine	14150035	FDA UDI	Class II	Active
Brigade	7501073	FDA UDI	Class II	Active
CoRoent	5299324P2	FDA UDI	Class II	Active
VuePoint	8980412P3	FDA UDI	Class II	Active
CoRoent	6508245CP2	FDA UDI	Class II	Active
CoRoent	6081330P2	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.