Hoffmann LRF

Hex Slotted Wire Bolt- Medium for Wire D1.5 to 2.0 mm

Registry build 21.09.26
17manufacturers in China registered for this device type
108catalogue numbers in this listing
11510(k) clearances naming this product code
15recalls on this code

Who Else Makes It

Concentrated in Jiangsu (6), Shanghai (4), Zhejiang (3). 13 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code KTT
Manufacturer City Province Registered as Device types
Apex (Guangzhou) Tools & Orthopedics Company Guangzhou Guangdong Contract manufacturer 62
Changzhou Biomet Medical Devices Co., Ltd. Changzhou Jiangsu Contract manufacturer 54
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
LX Precision Shanghai Co Ltd Shanghai Shanghai Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17
Turnxon Precision Co., Ltd. Dongguan Guangdong Contract manufacturer 17
Zibo Dante Co., Ltd. Zibo Shandong Contract manufacturer 17
Stryker Orthmed (Changzhou) Medical Instrument Co., Ltd. Changzhou Jiangsu Contract manufacturer 10
Hangzhou Sino-MIM Technology Co., Ltd. Hangzhou Zhejiang Contract manufacturer 6
Suzhou AND Science & Technology Development Corp. Zhangjiagang Jiangsu Contract manufacturer 5

Showing 12 of 17. All 17 manufacturers in China registered for Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

Record

Regulatory record for Hoffmann LRF
Listed by Stryker GmbH, Switzerland
FDA product code KTT
Device type Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Device class Class 2
Regulation 21 CFR 888.3030
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Record published 2026-07-15

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Moist Heat or Steam Sterilization
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Sizes Length 12 to 200 mm; width 23 mm; height 22 to 42 mm

Catalogue Numbers

Catalogue numbers for Hoffmann LRF
Catalogue number Size Per pack Status
4938-1-022 In distribution
4936-3-255 Diameter: 255.0 Millimeter In distribution
4936-6-155 Diameter: 155.0 Millimeter In distribution
4938-9-013 In distribution
4938-0-200 Length 200.0 mm In distribution
4937-1-180 Diameter: 180.0 Millimeter In distribution
4938-1-002 In distribution
4936-2-205 Diameter: 205.0 Millimeter In distribution
4937-6-130 Diameter: 130.0 Millimeter In distribution
4936-6-205 Diameter: 205.0 Millimeter In distribution
4938-2-002 In distribution
4936-0-105 Length 105.0 mm In distribution
4936-3-230 Diameter: 230.0 Millimeter In distribution
4936-3-050 In distribution
4937-5-180 Diameter: 180.0 Millimeter In distribution
4936-0-180 Diameter: 180.0 Millimeter In distribution
4938-2-004 In distribution
4938-3-205 In distribution
4937-7-155 Diameter: 155.0 Millimeter In distribution
4938-1-024 In distribution
4936-2-280 Diameter: 280.0 Millimeter In distribution
4938-3-201 In distribution
4936-1-305 Diameter: 305.0 Millimeter In distribution
4937-7-105 Diameter: 105.0 Millimeter In distribution
4938-9-012 In distribution
4938-1-100 Length 12.0 mm In distribution
4937-6-105 Diameter: 105.0 Millimeter In distribution
4937-6-180 Diameter: 180.0 Millimeter In distribution
4938-1-005 In distribution
4937-2-130 Diameter: 130.0 Millimeter In distribution
4937-1-105 Diameter: 105.0 Millimeter In distribution
4938-1-003 In distribution
4937-5-130 Diameter: 130.0 Millimeter In distribution
4936-3-180 Diameter: 180.0 Millimeter In distribution
4936-2-180 Diameter: 180.0 Millimeter In distribution
4937-1-205 Diameter: 205.0 Millimeter In distribution
4938-9-001 In distribution
4938-9-011 In distribution
4937-1-130 Diameter: 130.0 Millimeter In distribution
4936-3-030 In distribution
4938-3-200 In distribution
4936-3-130 Diameter: 130.0 Millimeter In distribution
4936-1-280 Diameter: 280.0 Millimeter In distribution
4938-1-004 In distribution
4937-2-205 Diameter: 205.0 Millimeter In distribution
4936-2-080 Diameter: 80.0 Millimeter In distribution
4938-1-200 In distribution
4938-2-003 In distribution
4938-2-005 In distribution
4936-3-205 Diameter: 205.0 Millimeter In distribution
4936-3-070 Length 51.0 mm In distribution
4936-6-130 Diameter: 130.0 Millimeter In distribution
4936-1-130 Diameter: 130.0 Millimeter In distribution
4937-7-205 Diameter: 205.0 Millimeter In distribution
4937-5-205 Diameter: 205.0 Millimeter In distribution
4936-1-255 Diameter: 255.0 Millimeter In distribution
4936-3-060 Height 22.0 mm In distribution
4938-9-002 In distribution
4938-1-023 In distribution
4938-0-150 Length 150.0 mm In distribution
4938-3-103 Screw Holes: 1.0 Holes In distribution
4937-1-155 Diameter: 155.0 Millimeter In distribution
4936-1-155 Diameter: 155.0 Millimeter In distribution
4936-6-180 Diameter: 180.0 Millimeter In distribution
4938-0-060 Length 60.0 mm In distribution
4939-9-022 In distribution
4938-1-050 Diameter: 6.0 Millimeter 8 In distribution
4936-2-155 Diameter: 155.0 Millimeter In distribution
4937-5-155 Diameter: 155.0 Millimeter In distribution
4936-1-105 Length 105.0 mm In distribution
4938-3-102 Screw Holes: 2.0 Holes In distribution
4936-3-020 In distribution
4936-0-155 Diameter: 155.0 Millimeter In distribution
4938-1-310 Length 22.0 mm In distribution
4938-1-001 In distribution
4936-2-230 Diameter: 230.0 Millimeter In distribution
4938-3-104 Screw Holes: 2.0 Holes In distribution
4938-9-100 In distribution
4936-1-180 Diameter: 180.0 Millimeter In distribution
4936-3-105 Diameter: 105.0 Millimeter In distribution
4937-2-105 Diameter: 105.0 Millimeter In distribution
4937-2-180 Diameter: 180.0 Millimeter In distribution
4938-1-021 In distribution
4936-0-130 Length 130.0 mm In distribution
4936-3-010 In distribution
4937-7-180 Diameter: 180.0 Millimeter In distribution
4936-2-130 Diameter: 130.0 Millimeter In distribution
4936-1-205 Diameter: 205.0 Millimeter In distribution
4937-7-130 Diameter: 130.0 Millimeter In distribution
4937-2-155 Diameter: 155.0 Millimeter In distribution
4936-0-205 Diameter: 205.0 Millimeter In distribution
4938-1-051 In distribution
4936-6-105 Diameter: 105.0 Millimeter In distribution
4938-1-300 Length 15.0 mm In distribution
4938-0-100 Length 100.0 mm In distribution
4936-1-230 Diameter: 230.0 Millimeter In distribution
4936-3-155 Diameter: 155.0 Millimeter In distribution
4937-5-105 Diameter: 105.0 Millimeter In distribution
4938-3-002 In distribution
4936-1-080 Diameter: 80.0 Millimeter In distribution
4937-6-205 Diameter: 205.0 Millimeter In distribution
4936-2-301 In distribution
4938-3-105 Screw Holes: 3.0 Holes In distribution
4936-2-105 Diameter: 105.0 Millimeter In distribution
4936-3-040 In distribution
4936-2-255 Diameter: 255.0 Millimeter In distribution
4938-0-063 In distribution
4937-6-155 Diameter: 155.0 Millimeter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Smart Correction Wishbone Medical Inc. 1,534
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Synthes Gmbh 880
LCP Synthes Gmbh 355
Orthex External Fixation System Orthopediatrics, Corp 353
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Sterilmed, Inc. 325
CHS Smith & Nephew, Inc. 321
Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component Stryker Sustainability Solutions 277
Hoffmann Stryker GmbH 239
Orthex Orthopediatrics, Corp 231
Orthex Vilex IN Tennessee, Inc. 221
Omega Stryker GmbH 212
eZ-Fix Orthopediatrics, Corp 207

Showing 12 of 530. All products under Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K253202 2025-12-19
K233741 2023-12-21
K203568 2021-02-01
K182968 2019-01-25
K163656 2017-04-14
K161753 2016-11-15
K153377 2016-04-11
K122284 2012-10-24
K121252 2012-07-25
K113327 2012-03-29
K111786 2012-01-26

Recalls

15 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
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 9,658 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 5,439 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 5,664 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 4,505 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 9,405 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 7,571 units
2026-07-01 Class II Device Design Potential cracking of the Hoffmann II Carbon Connecting Rods following cleaning and sterilization. 6,244 units
2024-05-09 Class II Process change control The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly. 39 devices
2023-02-07 Class II Process change control Stryker has identified a nonconformance in specific lots of Hoffmann LRF Bone Transport Struts. Specifically, the thread pitch is oversized at the distal end of the threaded rod, and as a result the distal ring fixation cannot be locked bet 488 units
2018-08-28 Class II Under Investigation by firm The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in p 1355 2021-02-04
2018-08-28 Class II Under Investigation by firm The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in p 832 2021-02-04
2018-08-28 Class II Under Investigation by firm The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in p 867 2021-02-04
2018-08-28 Class II Under Investigation by firm The press fit connection of the Angular Sleeve and pin of the U-Joint and Click Lock did not meet specification. A dimensional discrepancy of the bore hole of the Angular Sleeve may cause a reduced press fit of the pin. This can result in p 578 2021-02-04
2018-07-26 Class II Under Investigation by firm When creating a correction plan with the Correct Axial First button selected and the No. of corrections per day set to more than 1 (e.g., 2, 3, or 4), the Hexapod Software computes an erroneously accelerated correction plan for the axial 233 2020-05-26
2018-03-12 Class II Labeling mix-ups The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling 18 2020-05-21

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