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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 17 of 500

Device	Model / Reference	Registries	Class	Status
Tlif	6602011	FDA UDI	Class II	Active
XLIF Decade Plate	7140218	FDA UDI	Class II	Active
X-Core	6223012	FDA UDI	Class II	Active
Archon	8687242	FDA UDI	Class II	Active
Brigade	1577432	FDA UDI	Class II	Active
XLIF Decade Plate	1631395	FDA UDI	Class II	Active
Base	6953220	FDA UDI	Class II	Active
ReLine	11089060	FDA UDI	Class II	Active
VuePoint	8980134P	FDA UDI	Class II	Active
ReLine	24029555	FDA UDI	Class II	Active
Archon	8780412	FDA UDI	Class II	Active
CoRoent	6481250	FDA UDI	Class II	Active
Archon	8881518	FDA UDI	Class II	Active
ReLine	12160075	FDA UDI	Class II	Active
ReLine	11155135	FDA UDI	Class II	Active
ReLine	11045585	FDA UDI	Class II	Active
ReLine	10300708P	FDA UDI	Class II	Active
ReLine	3700035	FDA UDI	Class II	Active
ReLine	10000138	FDA UDI	Class I	Active
CoRoent	6840210	FDA UDI	Class II	Active
ReLine	11026530	FDA UDI	Class II	Active
Armada	8450155	FDA UDI	Class II	Active
CoRoent	5251304P2	FDA UDI	Class II	Active
CoRoent	6777216	FDA UDI	Class II	Active
Tlx	1742694	FDA UDI	Class II	Active
ReLine	13021135	FDA UDI	Class II	Active
ReLine	10000304	FDA UDI	Class I	Active
Gradient	7450500	FDA UDI	Class II	Active
CoRoent	6850107	FDA UDI	Class II	Active
ReLine	14155075	FDA UDI	Class II	Active
VuePoint	7907370	FDA UDI	Class I	Active
Base	6959150	FDA UDI	Class II	Active
ReLine	10001121	FDA UDI	Class I	Active
CoRoent	5142340P2	FDA UDI	Class II	Active
Precept	8884550	FDA UDI	Class II	Active
Halo	7893092	FDA UDI	Class II	Active
ReLine	11355035	FDA UDI	Class II	Active
ReLine	3724032	FDA UDI	Class II	Active
ReLine	24018530	FDA UDI	Class II	Active
ReLine	BETRELCCOREIMP	FDA UDI	Class II	Active
ReLine	3824520	FDA UDI	Class II	Active
CoRoent	5134302	FDA UDI	Class II	Active
ReLine	16026070	FDA UDI	Class II	Active
ReLine	13017045	FDA UDI	Class II	Active
Brigade	7932042	FDA UDI	Class II	Active
VuePoint	7903330	FDA UDI	Class II	Active
ReLine	16218570	FDA UDI	Class II	Active
CoRoent	5262320P2	FDA UDI	Class II	Active
ReLine	14546065	FDA UDI	Class II	Active
ReLine	14524020	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.