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Explore product specifications, available configurations, compatible instruments, and regulatory documentation for this product.

Home Joint Prostheses Femoral Condyle CR
Femoral Condyle CR
Femoral Condyle CR
  • Geasure Medical

  • 1

  • ISO 13485 \ CE \ FDA 510(k) Cleared \ Free Sale Certificate\ MDSAP

  • CoCrMo

  • Custom service supported

  • 7–14 Days (OEM: 15–30 Days)

  • Ethylene oxide sterilization

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CR Femoral Condyle Introduction

High-flexion femoral Condyle CR.jpg

The Geasure CR Femoral Condyle is the cruciate-retaining femoral component listed for Active High Flexion TKA System III. It is offered in left and right configurations across six sizes, from 4L/4R to 14L/14R, with ML and AP dimensions specified in the product catalog. It is intended to be selected as part of the corresponding System III configuration.

 CR Femoral Condyle Key Features

  • CR configuration: Identified in the catalog as the CR femoral-condyle option in Active High Flexion TKA System III. The catalog also lists a PS option in the same system.

  • Left and right options: Available in both L and R configurations, allowing buyers to distinguish side-specific product numbers.

  • Six listed sizes: Sizes run from 4 to 14 in even-numbered increments.

  • ML and AP dimensions provided: The catalog specifies both dimensions for each size to support product comparison and procurement review.

  • System-level component options: System III lists matching III-type tibial trays and CR, CRDF, and III-type polyethylene inserts. Confirm the exact pairing from current technical documentation before ordering.

  • High-flexion system positioning: The product catalog presents System III as a high-flexion TKA system. It does not establish a clinical outcome or a specific flexion result for this CR component.

CR Femoral Condyle Specifications

Product No.

Model / Size

ML (mm)

AP (mm)

Material

B770101

4L

58

50

CoCrMo

B770102

6L

62

55

B770103

8L

66

59

B770104

10L

70

62

B770105

12L

73

66

B770111

14L

76

70

B770106

4R

58

50

B770107

6R

62

55

B770108

8R

66

59

B770109

10R

70

62

B770110

12R

73

66

B770112

14R

76

70

The source labels the dimensions ML and AP; the table preserves those labels without assigning further definitions.

Compatible Components and Instruments

The 2026 joint product catalog lists the following components in Active High Flexion TKA System III:

Component

Catalog reference

Procurement note

III-type tibial tray

B7201 series

Verify size pairing against the current system chart.

CR polyethylene insert

B7801/B7802 series

Available in three sizes and thicknesses: 9 mm, 11 mm, and 13 mm.

CRDF polyethylene insert

B8001/B8002 series

Available in three sizes and thicknesses: 9 mm, 11 mm, and 13 mm.

III-type polyethylene insert

B7301/B7302 series

Available in three sizes and thicknesses: 9 mm, 11 mm, and 13 mm.

Bone cement stem

B7401/B7601 series

The specification is 9*90; the dimensions are 10 mm in diameter and either 40 mm or 55 mm in length. Please confirm the intended configuration.

Tibial plateau screw

B750101 / B600401

The listed specification is 9.

The catalog does not identify the instruments required for this CR femoral condyle. No cross-brand interchangeability is established by the available information.

Manufacturer Strengths

Geasure Medical’s current website describes the company as an orthopedic implant and surgical instrument manufacturer, lists Joint Prostheses as a product line, and states that the company supports OEM/ODM cooperation and operates under an ISO 13485 quality system. These are company-level statements, not confirmation of this component’s material, regulatory status, or product-specific certification. (orthogeasure.com)

Distributor and OEM/ODM Cooperation

Distributors, importers, and brand owners can submit the required CR size and product number, intended system configuration, estimated order quantity, target market, and any registration-document requirements. For OEM/ODM enquiries, include the requested changes and applicable technical or regulatory specifications so Geasure can assess the project scope. Product-specific customization availability and regulatory documentation should be confirmed during technical review.

CR Femoral Condyle FAQ

What is the CR femoral condyle?
It is the CR femoral component listed in Geasure’s Active High Flexion TKA System III. The catalog also lists a PS femoral component option for System III.

What sizes are available?
The catalog lists sizes 4, 6, 8, 10, 12, and 14 for both left (L) and right (R) configurations. Product numbers and ML/AP dimensions are shown in the specification table.

What material and surface finish does it use?
The reviewed product catalog does not specify the material or surface finish for the B7701 CR femoral condyle. Request the current controlled technical specification before adding these details to purchasing documents.

Which components are listed with this femoral condyle?
The catalog lists the System III tibial tray and CR, CRDF, and III-type polyethylene inserts, as well as bone cement stems and tibial plateau screws. Confirm exact size combinations using the current compatibility chart.

Are dedicated surgical instruments specified?
Dedicated instruments for this component are not identified in the reviewed catalog pages. Request the current instrument list and confirm that it corresponds to the selected System III configuration.

Can Geasure provide certification or registration documents for this product?
The documents required and the product’s market status must be checked for the specific product and target country. Company-level certificates do not by themselves establish that this femoral condyle has a particular clearance or registration.

What information should distributors include in an enquiry?
Provide the product number and size, left/right configuration, intended System III component pairing, estimated quantity, target market, required regulatory documents, and any OEM/ODM request. This helps the team assess the enquiry against the relevant technical and regulatory requirements.