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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
Address: —
Website: —
LinkedIn: —
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: —
DUNS Number: 202981171

Catalogue (155)

Page 2 of 4

Device	Model / Reference	Registries	Class	Status
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L60mm	037-131-060	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L32mm	037-106-032	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L48mm	037-131-048	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L46mm	037-106-046	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L62mm	037-131-062	FDA UDI	Class II	Active
Bodycad Unicompartmental Knee System	010003	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L46mm	037-131-046	FDA UDI	Class II	Active
Fine Osteotomy disposable instruments - Distal femur	015-330-601	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L34mm	037-106-034	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L62mm	037-106-062	FDA UDI	Class II	Active
3.2mm Pre-Drill Sleeve	027-107	FDA UDI	Class I	Active
Fine Osteotomy system - Proximal tibia	015-410-003	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-106	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L38mm	037-131-038	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L50mm	037-106-050	FDA UDI	Class II	Active
Fine osteotomy HB 6.5 Cancellous Bone Screw - L60mm	037-112-060	FDA UDI	Class II	Active
Fine Osteotomy system - Distal femur	015-330-106	FDA UDI	Class II	Active
BC Reflex Uni	018-001	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L42mm	037-106-042	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Bone Screw - L40mm	037-131-040	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L64mm	037-131-064	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L60mm	037-106-060	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-106	FDA UDI	Class II	Active
Fine Osteotomy system - Distal femur	015-330-001	FDA UDI	Class II	Active
BC Reflex Uni Reusable Surgical Instrument Set	027-003	FDA UDI	Class I	Active
Fine Osteotomy implants - Proximal tibia	015-410-103	FDA UDI	Class II	Active
Bone Spreader	027-401	FDA UDI	Class I	Active
Fine Osteotomy implants - Proximal tibia	015-410-107	FDA UDI	Class II	Active
Fine Osteotomy system - Distal femur	015-330-002	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-101	FDA UDI	Class II	Active
Fine osteotomy HB 6.5 Cancellous Bone Screw - L40mm	037-112-040	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L36mm	037-131-036	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L56mm	037-106-056	FDA UDI	Class II	Active
Fine Osteotomy disposable instruments - Proximal tibia	015-410-601	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-102	FDA UDI	Class II	Active
Fine Osteotomy implants - Distal femur	015-330-104	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-104	FDA UDI	Class II	Active
Drill Bit Ø2.0mm x 80 mm	027-101-080	FDA UDI	Class I	Active
Fine Osteotomy disposable instruments - Distal femur	015-330-603	FDA UDI	Class II	Active
Torque Limiting Adaptor, AO Connect, 4 N-m	027-203	FDA UDI	Class I	Active
Fine Osteotomy implants - Distal femur	015-330-107	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L58mm	037-131-058	FDA UDI	Class II	Active
Fine osteotomy Locking HA 4.5 Cortical Bone Screw - L50mm	037-131-050	FDA UDI	Class II	Active
Fine Osteotomy implants - Proximal tibia	015-410-103	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L52mm	037-106-052	FDA UDI	Class II	Active
Fine Osteotomy implants - Distal femur	015-330-102	FDA UDI	Class I	Active
Fine Osteotomy system - Distal femur	015-330-004	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L54mm	037-106-054	FDA UDI	Class II	Active
Fine osteotomy HA 4.5 Cortical Bone Screw - L48mm	037-106-048	FDA UDI	Class II	Active
Fine Osteotomy system - Distal femur	015-330-007	FDA UDI	Class II	Active

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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.