Tmini® Guide Block Kit Compatible With Stryker® Triathlon® Knee System (10ea)

2 catalogue numbers from 109900-M, listed by Think Surgical Inc., United States, under Orthopedic Stereotaxic Instrument. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
2catalogue numbers in this listing
19510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Guangdong (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 OLO
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53

Record

Regulatory record for Tmini® Guide Block Kit compatible with Stryker® Triathlon® Knee System (10ea)
Listed by Think Surgical Inc., United States
FDA product code OLO
Device type Orthopedic Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K253661
Record published 2026-03-02

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number

Catalogue Numbers

Catalogue numbers for Tmini® Guide Block Kit compatible with Stryker® Triathlon® Knee System (10ea)
Catalogue number Size Status
109900-M In distribution
110025 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Valence Robotic Navigation System Alphatec Spine, Inc. 813
Olympic Astura Medical 684
Excelsius GPS Globus Medical, Inc. 383
Orthopedic Stereotaxic Instrument Medtronic Navigation, Inc. 356
Masada Astura Medical 335
Excelsiusgps Globus Medical, Inc. 297
Invictus Alphatec Spine, Inc. 235
OrthAlign Plus OrthAlign, Inc. 210
Arvis ® Kico Knee Innovation Company 174
OMNIBotics Omni Life Science, Inc. 150
CD Horizon® Spinal System Medtronic Sofamor Danek, Inc. 137
Navigation Instruments VB Spine LLC 135

Showing 12 of 1,127. All products under Orthopedic Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K261024 2026-07-24
K260010 2026-03-03
K253661 2025-12-22
K252544 2025-10-10
K250877 2025-06-20
K243481 2025-01-06
K243285 2024-11-15
K242264 2024-08-23
K241031 2024-07-12
K232802 2023-10-12
K230202 2023-04-25
K210668 2021-04-01
K203040 2020-11-13
K201255 2020-06-10
K193135 2019-12-11
K191369 2019-10-08
K170430 2017-03-06
K162195 2016-09-14
K153647 2016-02-16

Recalls

3 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2026-05-08 Class II Process control Due to manufacturing/design issue where the knob on the tracking array may loosen causing potential misalignment of the array. 360 devices
2024-02-12 Class II Device Design There is a galling effect (cold-weld) caused by friction between the array fixation pins and the TMINI array guide holes due to insufficient clearance between the outer diameter of the fixation pins and the inner diameter of the TMINI array 16
2018-03-30 Class II Process control There is a potential for the cutter head to detach from the cutter shaft. 951 2020-01-24

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