Pangea

Tray for Interprosthetic Femur Targeters

Registry build 21.09.26
53manufacturers in China registered for this device type
69catalogue numbers in this listing
2510(k) clearances naming this product code
3recalls on this code

Who Else Makes It

Concentrated in Jiangsu (24), Guangdong (7), Zhejiang (6). 29 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LXH
Manufacturer City Province Registered as Device types
Zhejiang Biomet Medical Products Co., Ltd. Jinhua Zhejiang Contract manufacturer 74
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Canwell Medical Co., Ltd. Jinhua Zhejiang Contract manufacturer 42
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
B.Braun Medical (Suzhou) Co,.Ltd Suzhou Jiangsu Contract manufacturer 37
Suzhou Elite Precision Machinery Co., Ltd. Kunshan Jiangsu Contract manufacturer 35
Xinhua Healthcare Industry Co., Limited Zibo Shandong Contract manufacturer 30
Guangzhou Aquila Precise Tools Limited Guangzhou Guangdong Contract manufacturer 28
B-ONE Medical (Suzhou) Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Suzhou Jinsheng Plastic Co., Ltd. Suzhou Jiangsu Contract manufacturer 23
Stryker (Suzhou) Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 19
Suzhou Ahno Medical Devices Co., Ltd. Suzhou Jiangsu Contract manufacturer 17

Showing 12 of 53. All 53 manufacturers in China registered for Orthopedic Manual Surgical Instrument

Record

Regulatory record for Pangea
Listed by Stryker GmbH, Switzerland
FDA product code LXH
Device type Orthopedic Manual Surgical Instrument
Device class Class 1
Regulation 21 CFR 888.4540
Establishment Contract manufacturer, Specification developer, Complaint-file establishment, Manufacturer
Premarket notification Exempt
Record published 2023-06-13
Record revised 2026-05-27 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Sizes Length 32 to 262 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Pangea
Catalogue number Size Status
940606 In distribution
940569 Screw Head: 20.0 Torx In distribution
542133 Length 185.0 mm In distribution
940615 In distribution
706409 Length 136.0 mm In distribution
940607 In distribution
542113 Length 160.0 mm In distribution
542069 Screw Head: 20.0 Torx In distribution
542008 Diameter: 2.0 Millimeter In distribution
542025 Screw Head: 15.0 Torx In distribution
542036S Length 100.0 mm In distribution
940598 In distribution
542028 Screw Head: 15.0 Torx In distribution
940562 In distribution
542068 Screw Head: 20.0 Torx In distribution
940568 Screw Head: 20.0 Torx In distribution
542060 Length 60.0 mm In distribution
542116 In distribution
542005 Screw Head: 8.0 Torx In distribution
542009 Diameter: 2.5 Millimeter In distribution
542006 Screw Head: 8.0 Torx In distribution
940618 In distribution
703919 Screw Head: 10.0 Torx In distribution
542015 Screw Head: 8.0 Torx In distribution
542112 Length 134.0 mm In distribution
542098 Screw Head: 8.0 Torx In distribution
706442 Length 215.0 mm In distribution
706441 Length 190.0 mm In distribution
940605 In distribution
940567 Screw Head: 20.0 Torx In distribution
940599 In distribution
542035 Screw Head: 15.0 Torx In distribution
706420 In distribution
706439 Length 185.0 mm In distribution
542138 Length 34.0 mm In distribution
706404 In distribution
542030 Diameter: 2.5 Millimeter In distribution
542137 Length 262.0 mm In distribution
706418 Length 140.0 mm In distribution
542064 Diameter: 3.2 Millimeter In distribution
542014 Screw Head: 8.0 Torx In distribution
542027 Screw Head: 15.0 Torx In distribution
542061 Diameter: 2.0 Millimeter In distribution
542010 Diameter: 2.7 Millimeter In distribution
706416 In distribution
542058 Screw Head: 20.0 Torx In distribution
542065 Screw Head: 20.0 Torx In distribution
940617 In distribution
542118 Length 32.0 mm In distribution
542026 Diameter: 2.5 Millimeter In distribution
940564 Screw Head: 20.0 Torx In distribution
542164 In distribution
542163 In distribution
706405 Length 125.0 mm In distribution
703918 Screw Head: 8.0 Torx In distribution
706419 Length 136.0 mm In distribution
542059 Diameter: 3.2 Millimeter In distribution
940597 In distribution
542062 Diameter: 3.2 Millimeter In distribution
706440 Length 205.0 mm In distribution
542063 Diameter: 4.3 Millimeter In distribution
940563 In distribution
940561 In distribution
542036 Diameter: 1.6 Millimeter In distribution
542034 Screw Head: 15.0 Torx In distribution
542099 Screw Head: 20.0 Torx In distribution
542117 Length 209.0 mm In distribution
542136 Length 205.0 mm In distribution
940616 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Razek Equipamentos Razek Equipamentos Ltda 11,578
Orthopedic Manual Surgical Instrument Globus Medical, Inc. 4,784
Instrument Howmedica Osteonics Corp 4,539
Orthopedic Manual Surgical Instrument Ortho Development Corp. 4,076
Knee Instruments Medacta International SA 3,944
Kyocera Medical Technologies, Inc. Kyocera Medical Technologies, Inc. 3,420
Arthrex® Arthrex, Inc. 3,106
Spine Instruments Medacta International SA 2,892
Orthopedic Manual Surgical Instrument Medtronic Sofamor Danek, Inc. 2,766
Hip Instruments Medacta International SA 1,904
Medtronic Reusable Instruments Medtronic Sofamor Danek, Inc. 1,756
ReLine Nuvasive, Inc. 1,208

Showing 12 of 9,501. All products under Orthopedic Manual Surgical Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K941605 1994-08-05
K843942 1985-04-15

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
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 1588 units
2025-03-28 Class II Device Design The metal ring at the end of the Guide Wire with Ruler Tube may detach from the main body of the instrument during use in surgery. 6407 units
2017-11-09 Class II Environmental control Lack of sterility assurance as bioburden levels were found to be higher than internal acceptable rates. 320 2019-04-16

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