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SiJoin T3 Titanium

FDA UDI

Class II (US FDA UDI)

by Vgi Medical, Llc

Identity

Trade Name
SiJoin T3 Titanium FDA UDI
Generic Name
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated FDA UDI
Device Name
SiJoin T3 Titanium 22x40x5 FDA UDI
Model / Reference
VG-SJ-T3-22240 FDA UDI
Description
SiJoin T3 Titanium 22x40x5 FDA UDI

Identifiers

Catalog Number
VGSJT322240 FDA UDI
Primary DI / UDI-DI
B387VGSJT3222400 FDA UDI
510(k) Number
K213815 FDA UDI
FDA Product Code
OUR FDA UDI
GMDN Term
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Width — 22 Millimeter FDA UDI
Length — 40 Millimeter FDA UDI
Height — 5 Millimeter FDA UDI

Category: Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated

SiJoin T3 Titanium by Vgi Medical, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Vgi Medical, Llc

Sources (1)

  • FDA UDI 52ff6fc4-69ed-4602-86b3-da24feb436a7 37 fields · synced May 31, 2026