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Laboratoires Bodycad Inc · Knee implants
FDA device identifier records list Bodycad Unicompartmental Knee System under Laboratoires Bodycad Inc. This page lists 1 device model identifiers in Knee implants; source families may also contain components and instruments. UDI listing identifies products; it does not establish FDA approval or recall status.
No recall records are linked to this device in MedWatcher’s published dataset. Coverage is limited, and newer records may not yet be included.
Source checks below cover individual records. A manufacturer product-page check confirms device identity; it does not confirm recall status.
No recall records are currently linked here. This is not a complete recall search or a statement that the product is safe or appropriate for you. Search the FDA recall database using the device name and manufacturer, then compare the model and serial or lot numbers with your device.
These identity records can cover devices, accessories or software associated with this name. They do not establish FDA approval or identify which products are affected by a recall. Compare your label with the official record; recall scope is listed separately below.
Showing 1–1 of 1 identity records
| Model / version | Catalogue number | Primary device identifier |
|---|---|---|
| 010003 | 010003 | 00688346010008 — FDA record (opens in a new tab) |