Ifuse Torq Implant System-Driver Sleeve 2

Driver Sleeve 2

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
27510(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 iFuse Torq Implant System-Driver Sleeve 2
Listed by SI-Bone, Inc., United States
FDA product code OUR
Device type Sacroiliac Joint Fixation
Device class Class 2
Regulation 21 CFR 888.3040
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K203247
Record published 2021-03-08
Record revised 2022-11-28 (version 2)

Specifications

Specifications
MRI safety MR Conditional
Sterilisation Moist Heat or Steam Sterilization
Prescription Prescription only
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for iFuse Torq Implant System-Driver Sleeve 2
Catalogue number Size Status
400262 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
K253488 2026-02-11
K253094 2025-10-09
K241504 2024-08-19
K241574 2024-07-02
K233508 2024-01-26
K231689 2023-06-30
K222774 2022-12-22
K222605 2022-09-29
K213667 2022-06-10
K220195 2022-05-26
K203247 2021-02-25
K193524 2020-03-31
K190230 2019-04-03
K182983 2018-11-27
K162733 2017-03-10
K160652 2016-06-03
K152681 2016-03-01
K151718 2015-10-29
K150875 2015-07-22
K150714 2015-04-17
K141049 2014-07-23
K131405 2013-10-16
K123850 2013-04-01
K122074 2012-10-12
K110838 2011-04-21
K092375 2009-09-04
K080398 2008-11-26

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