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Laboratoires Bodycad Inc

Last updated May 23, 2026

What Laboratoires Bodycad Inc makes

Laboratoires Bodycad Inc manufactures orthopaedic fixation hardware, including non-bioabsorbable plates and screws for internal bone stabilization, as well as unicondylar knee prostheses for partial joint replacement. Their portfolio also includes reusable surgical tools such as fluted drill bits, osteotomes, screwdrivers, and general surgical procedure kits, alongside custom-made surgical guides for orthopaedic and craniofacial procedures. Specific products include cortical and cancellous bone screws, distal femur and proximal tibia osteotomy systems, and precision drill bits for orthopaedic surgery.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are intended for use in the United States, adhering to applicable regulatory requirements for surgical instruments and orthopaedic implants.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country: US
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EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 202981171

Catalogue (155)

Page 4 of 4

Device	Model / Reference	Registries	Class	Status
Drill Bit Ø2.0mm x 110 mm	027-101-110	FDA UDI	Class I	Active
Fine Osteotomy system - Distal femur	015-330-006	FDA UDI	Class II	Active
Fine osteotomy HB 6.5 Cancellous Bone Screw - L75mm	037-112-075	FDA UDI	Class II	Active
Fine Osteotomy system - Distal femur	015-330-005	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L52mm	037-131-052	FDA UDI	Class II	Active

Related Companies

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Laboratoires Bodycad Inc. has one FDA recall record initiated on 2021-07-02, which is recorded as terminated. The recall was due to a risk of breakage of the torque limiting adaptor if used counterclockwise and the restriction that it must not be used with a power tool, as no test data validated this use.

AI-generated summary of the recall records listed below. It describes what the records state and is not an assessment of this manufacturer.

Date	Recall No.	Class	Status	Reason
Jul 2, 2021	Z-0244-2022	—	terminated	There is a risk of breakage of the torque limiting adaptor if used counterclockwise and it must not be used with a power tool due to no test data validating this use.