Skip to content

Bodycad Laboratories, Inc.

CanadaFDA applicant, unverified FDA FEI 3012086398

Devices
16
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA FEI

What Bodycad Laboratories, Inc. makes

Bodycad Laboratories, Inc. manufactures orthopedic implants, including custom-cut bone osteotomy devices (Fine Osteotomy) and total and unicompartmental knee replacement systems (Bodycad Unicompartmental Knee System, BC Reflex Uni Knee System). Their portfolio also includes tibial tuberosity osteotomy tools (Fine TTO), designed for surgical procedures on the knee and lower limb.

The company’s devices are classified as Class II under FDA regulations and are authorised through the 510(k) pathway. These products are listed in the FDA’s 510(k) database, reflecting their compliance with US medical device regulations. The manufacturer operates from the United States.

AI-generated from registry data, 19 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue16

Newest first, rows 1-16 of 16

Search and filter all 16 devices
Skip device list

  • Fine Osteotomy™ Ref K240066

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine Osteotomy™ Ref K253300

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bodycad Unicompartmental Knee System Ref K163700

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine TTO™ Ref K250394

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • BC Reflex Uni Knee System Ref K211895

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine Osteotomy™ Ref K250923

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine Osteotomy™ Ref K240703

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bodycad Unicompartmental Knee System Ref K191150

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine Osteotomy™ Ref K241356

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • BC Reflex Uni Knee System Ref K191996

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Bodycad Unicompartmental Knee System Ref K181302

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • Fine Osteotomy™ Ref K231314

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • FINE Osteotomy Ref K211646

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • BC Reflex Uni Knee System Ref K212307

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • FINE Osteotomy around the knee Ref K193614

    Active Regimes: 510(k) Registry: 510(k) Class:II

  • BC Reflex Uni Knee System Ref K203697

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-16 of 16

Company details

FDA FEI number
3012086398
Address
2035 rue du Haut-Bord, Quebec

Frequently asked questions

How many devices does Bodycad Laboratories, Inc. have in the registry?

The registry currently lists 16 devices for Bodycad Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bodycad Laboratories, Inc.'s devices?

Among its 16 most recently registered devices, Bodycad Laboratories, Inc. has devices listed in FDA 510(k) (16 devices).

What risk classes do Bodycad Laboratories, Inc.'s devices fall under?

Among its 16 most recently registered devices, the classes recorded for Bodycad Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Bodycad Laboratories, Inc. in the registry?

The most recently registered devices listed for Bodycad Laboratories, Inc. include Fine Osteotomy™, Bodycad Unicompartmental Knee System, Fine TTO™ and BC Reflex Uni Knee System.

Generated automatically from registry data and not verified by a human reviewer.