SiCure Sacroiliac Joint Fusion System

Sacroiliac Joint Fusion Implant, 9.5mm DIA. x 50mm LGTH.

Registry build 21.09.26
3manufacturers in China registered for this device type
14catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Guangdong (1), Shandong (1), Jiangsu (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code OUR
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Autocam Medical Devices (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 9

Record

Regulatory record for SiCure Sacroiliac Joint Fusion System
Listed by Alevio, LLC, United States
FDA product code OUR
Device type Sacroiliac Joint Fixation
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Manufacturer
510(k) K141106
Record published 2016-09-24
Record revised 2022-11-28 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Outer diameter 9.5 to 11 mm; length 35 to 60 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for SiCure Sacroiliac Joint Fusion System
Catalogue number Size Status
900.11.40 Length 40 mm In distribution
900.095.50 Length 50 mm In distribution
900.095 Outer Diameter 9.5 mm In distribution
900.11.55 Length 55 mm In distribution
900.095.60 Length 60 mm In distribution
900.11.60 Length 60 mm In distribution
900.095.45 Length 45 mm In distribution
900.11.50 Length 50 mm In distribution
900.095.35 Length 35 mm In distribution
900.11.45 Length 45 mm In distribution
900.095.40 Length 40 mm In distribution
900.11 Outer Diameter 11 mm In distribution
900.095.55 Length 55 mm In distribution
900.11.35 Length 35 mm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
SI-LOK Globus Medical, Inc. 666
Sacroiliac Joint Fusion System Genesys Orthopedics Systems, LLC 356
SIros-X Genesys Orthopedics Systems, LLC 353
PathLoc- SI Joint Fusion System L&K Biomed Co., Ltd. 229
ARx SAI Life Spine 224
Unity Diomedical Co., Ltd. 198
SImmetry SI Joint Fusion System Tenon Medical, Inc. 173
M.u.s.t. Sacral Iliac Screw and Pelvic Trauma System Medacta International SA 170
Integrity-SI Fusion System Lincotek Medical, LLC 160
Zespin SI Joint Fusion System Aegis Spine 150
M.u.s.t. Sacral Iliac Screw System Medacta International SA 142
Simmetry Sivantage 123

Showing 12 of 534. All products under Sacroiliac Joint Fixation

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K231951 2023-07-28
K223819 2023-01-18

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer