Is this your brand? Sign in to claim ownership.

VGI MEDICAL, LLC

Last updated May 27, 2026

What VGI MEDICAL, LLC makes

VGI Medical, LLC manufactures polymeric spinal interbody fusion cages designed for intervertebral disc replacement and spinal stabilization. Their portfolio also includes sacroiliac joint implants for transarticular fixation and arthrodesis, as well as orthopaedic alignment tools for surgical precision in spinal procedures.

The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
Address: —
Website: vgimedical.com
LinkedIn: —
Facebook: —
Email: [email protected]
Phone: 727-565-1235
PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 019936692

Catalogue (282)

Page 6 of 6

Device	Model / Reference	Registries	Class	Status
VerteLP Interbody Fusion Device	VG-LP-18X50X10	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X70X15	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X55X10	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X45X8	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X55X15	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X65X13(7)	FDA UDI	Class II	Active
SiJoin T3 Titanium	VG-SJ-T3-22240	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X60X9	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X55X10(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X55X9(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X50X12(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X60X14(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X45X12(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X60X8	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X60X12(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X40X14(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X55X17	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X45X14	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X50X8	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X55X11	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X65X12(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X45X11	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X70X13(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X65X11(7)	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-22X50X14	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X50X11	FDA UDI	Class II	Active
VerteLP Interbody Fusion Device	VG-LP-18X50X10(7)	FDA UDI	Class II	Active
SiJoin T4 Titanium	VG-SJ-T4-22235	FDA UDI	Class II	Active
SiJoin T3 Titanium	VG-SJ-T3-21630	FDA UDI	Class II	Active
SiJoin T4 Titanium	VG-SJ-T4-21620	FDA UDI	Class II	Active
SiJoin T4 Titanium	VG-SJ-T4-22240	FDA UDI	Class II	Active
SiJoin®T3	K213815	FDA 510(k)	Class II	Active

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

VGI Medical, LLC has one FDA recall record initiated on 2018-04-09, which is marked as terminated. The recall pertains to an automated cleaning process for the VerteLP Instrument Tray that was not validated as described in the instructions for use (IFU).

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Apr 9, 2018	Z-2100-2018	—	terminated	IFU contained an automated cleaning process for the VerteLP Instrument Tray that was not validated